Related gene-specific medical variations for Gene (Select 80036) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3573576	NM_001366145.2(TRPM3):c.4471C>A (p.Leu1491Ile)	KLF9-DT, TRPM3 (L1316I +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3462125	NM_001366145.2(TRPM3):c.4853G>C (p.Arg1618Thr)	KLF9-DT, TRPM3 (R1453T +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3462119	NM_001366145.2(TRPM3):c.4559C>T (p.Thr1520Ile)	KLF9-DT, TRPM3 (T1345I +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3462117	NM_001366145.2(TRPM3):c.4022C>A (p.Thr1341Asn)	KLF9-DT, TRPM3 (T1166N +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3462116	NM_001366145.2(TRPM3):c.4763T>C (p.Val1588Ala)	KLF9-DT, TRPM3 (V1576A +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3462115	NM_001366145.2(TRPM3):c.3791G>A (p.Arg1264Gln)	KLF9-DT, TRPM3 (R1099Q +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3462113	NM_001366145.2(TRPM3):c.4318G>A (p.Glu1440Lys)	KLF9-DT, TRPM3 (E1287K +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3391096	NM_001366145.2(TRPM3):c.2672C>A (p.Ala891Glu)	TRPM3 (A716E +12 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures	GUncertain significance
Select item 3390510	NM_001366145.2(TRPM3):c.4681G>A (p.Asp1561Asn)	KLF9-DT, TRPM3 (D1386N +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3373241	NM_001366145.2(TRPM3):c.4933G>A (p.Glu1645Lys)	KLF9-DT, TRPM3 (E1470K +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3371817	NM_001366145.2(TRPM3):c.5044_5045delinsGA (p.Arg1682Glu)	KLF9-DT, TRPM3 (R1507E +9 more)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 3369979	NM_001366145.2(TRPM3):c.4718C>T (p.Ala1573Val)	TRPM3, KLF9-DT (A1398V +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3369049	NM_001366145.2(TRPM3):c.4540A>C (p.Ser1514Arg)	KLF9-DT, TRPM3 (S1339R +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3365724	NM_001366145.2(TRPM3):c.3720G>A (p.Met1240Ile)	KLF9-DT, TRPM3 (M1065I +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3364206	NM_001366145.2(TRPM3):c.3873C>A (p.Asn1291Lys)	KLF9-DT, TRPM3 (N1116K +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363628	NM_001366145.2(TRPM3):c.3680A>T (p.Asp1227Val)	KLF9-DT, TRPM3 (D1052V +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3362446	NM_001366145.2(TRPM3):c.308T>C (p.Ile103Thr)	TRPM3 (I103T +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures	GUncertain significance
Select item 3362273	NM_001366145.2(TRPM3):c.3658G>A (p.Asp1220Asn)	TRPM3 (D1045N +12 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures	GUncertain significance
Select item 3361718	NM_001366145.2(TRPM3):c.3517C>G (p.Leu1173Val)	TRPM3 (L1008V +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361237	NM_001366145.2(TRPM3):c.3593A>G (p.Asp1198Gly)	TRPM3 (D1023G +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3361199	NM_001366145.2(TRPM3):c.454A>G (p.Lys152Glu)	TRPM3 (K152E +1 more)	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GUncertain significance
Select item 3360716	NM_001366145.2(TRPM3):c.2884C>T (p.Leu962Phe)	TRPM3 (L787F +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3343527	NM_001366145.2(TRPM3):c.4780T>G (p.Cys1594Gly)	KLF9-DT, TRPM3 (C1419G +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3343088	NM_001366145.2(TRPM3):c.3701C>T (p.Ser1234Leu)	KLF9-DT, TRPM3 (S1059L +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3329224	NM_001366145.2(TRPM3):c.4223C>T (p.Pro1408Leu)	KLF9-DT, TRPM3 (P1233L +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3329223	NM_001366145.2(TRPM3):c.3665T>A (p.Phe1222Tyr)	KLF9-DT, TRPM3 (F1210Y +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3329221	NM_001366145.2(TRPM3):c.4660G>A (p.Ala1554Thr)	KLF9-DT, TRPM3 (A1379T +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3329219	NM_001366145.2(TRPM3):c.5069C>T (p.Ser1690Phe)	KLF9-DT, TRPM3 (S1537F +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3329218	NM_001366145.2(TRPM3):c.4793G>A (p.Arg1598Gln)	KLF9-DT, TRPM3 (R1458Q +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3238765	NM_001366145.2(TRPM3):c.4208C>T (p.Pro1403Leu)	KLF9-DT, TRPM3 (P1228L +9 more)	Single nucleotide variant (missense variant +1 more)	Cataract 50 with or without glaucoma	GUncertain significance
Select item 3236575	NM_001366145.2(TRPM3):c.4698G>T (p.Arg1566Ser)	KLF9-DT, TRPM3 (R1391S +9 more)	Single nucleotide variant (missense variant +1 more)	Neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures	GUncertain significance
Select item 3183338	NM_001366145.2(TRPM3):c.4970C>A (p.Ala1657Glu)	KLF9-DT, TRPM3 (A1482E +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183337	NM_001366145.2(TRPM3):c.4922T>G (p.Val1641Gly)	KLF9-DT, TRPM3 (V1476G +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183336	NM_001366145.2(TRPM3):c.4768G>T (p.Asp1590Tyr)	KLF9-DT, TRPM3 (D1425Y +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183335	NM_001366145.2(TRPM3):c.4687A>G (p.Ile1563Val)	KLF9-DT, TRPM3 (I1410V +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183334	NM_001366145.2(TRPM3):c.4567C>G (p.Leu1523Val)	KLF9-DT, TRPM3 (L1358V +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183333	NM_001366145.2(TRPM3):c.4544G>A (p.Arg1515His)	KLF9-DT, TRPM3 (R1375H +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183332	NM_001366145.2(TRPM3):c.4412T>C (p.Ile1471Thr)	KLF9-DT, TRPM3 (I1306T +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183331	NM_001366145.2(TRPM3):c.4352C>T (p.Ala1451Val)	KLF9-DT, TRPM3 (A1276V +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183330	NM_001366145.2(TRPM3):c.4307T>C (p.Leu1436Pro)	KLF9-DT, TRPM3 (L1271P +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183329	NM_001366145.2(TRPM3):c.4286T>C (p.Leu1429Pro)	KLF9-DT, TRPM3 (L1279P +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3183328	NM_001366145.2(TRPM3):c.3977G>A (p.Ser1326Asn)	KLF9-DT, TRPM3 (S1163N +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3183327	NM_001366145.2(TRPM3):c.3967C>A (p.Leu1323Ile)	KLF9-DT, TRPM3 (L1158I +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3183326	NM_001366145.2(TRPM3):c.3881G>A (p.Arg1294His)	KLF9-DT, TRPM3 (R1119H +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3183325	NM_001366145.2(TRPM3):c.3880C>T (p.Arg1294Cys)	KLF9-DT, TRPM3 (R1154C +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3183324	NM_001366145.2(TRPM3):c.3865G>A (p.Glu1289Lys)	KLF9-DT, TRPM3 (E1304K +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3059561	NM_001366145.2(TRPM3):c.3575-7del	KLF9-DT, TRPM3	Deletion (intron variant)	TRPM3-related disorder	GBenign
Select item 3057944	NM_001366145.2(TRPM3):c.4938C>T (p.Arg1646=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 3048440	NM_001366145.2(TRPM3):c.4477G>C (p.Glu1493Gln)	KLF9-DT, TRPM3 (E1318Q +9 more)	Single nucleotide variant (missense variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 3045822	NM_001366145.2(TRPM3):c.4440C>T (p.Asp1480=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 3044121	NM_001366145.2(TRPM3):c.3831G>T (p.Thr1277=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant)	TRPM3-related disorder	GBenign
Select item 3042958	NM_001366145.2(TRPM3):c.4317C>T (p.Gly1439=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 3042561	NM_001366145.2(TRPM3):c.3810C>A (p.Asp1270Glu)	KLF9-DT, TRPM3 (D1095E +12 more)	Single nucleotide variant (missense variant)	TRPM3-related disorder	GLikely benign
Select item 3042146	NM_001366145.2(TRPM3):c.4889A>T (p.Asn1630Ile)	KLF9-DT, TRPM3 (N1455I +9 more)	Single nucleotide variant (missense variant +1 more)	TRPM3-related disorder	GBenign
Select item 3040634	NM_001366145.2(TRPM3):c.4296C>T (p.Ser1432=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 3039881	NM_001366145.2(TRPM3):c.4642G>A (p.Gly1548Arg)	KLF9-DT, TRPM3 (G1373R +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3039489	NM_001366145.2(TRPM3):c.4919C>T (p.Thr1640Ile)	KLF9-DT, TRPM3 (T1465I +9 more)	Single nucleotide variant (missense variant +1 more)	TRPM3-related disorder	GBenign
Select item 3033476	NM_001366145.2(TRPM3):c.3708-7C>T	KLF9-DT, TRPM3	Single nucleotide variant (intron variant)	TRPM3-related disorder	GLikely benign
Select item 3033457	NM_001366145.2(TRPM3):c.5070C>G (p.Ser1690=)	KLF9-DT, TRPM3	Single nucleotide variant (synonymous variant +1 more)	TRPM3-related disorder	GLikely benign
Select item 2973494	NM_001366145.2(TRPM3):c.3999G>T (p.Glu1333Asp)	KLF9-DT, TRPM3 (E1180D +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2788259	NC_000009.12:g.70810008C>T	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2659249	NM_001366145.2(TRPM3):c.3708-6G>A	KLF9-DT, TRPM3	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2659248	NM_001366145.2(TRPM3):c.3860G>A (p.Arg1287Gln)	KLF9-DT, TRPM3 (R1112Q +12 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2659247	NM_001366145.2(TRPM3):c.4406G>T (p.Arg1469Leu)	KLF9-DT, TRPM3 (R1294L +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2659246	NM_001366145.2(TRPM3):c.4970C>T (p.Ala1657Val)	KLF9-DT, TRPM3 (A1482V +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2637530	NM_001366145.2(TRPM3):c.3991G>T (p.Gly1331Cys)	KLF9-DT, TRPM3 (E1178* +17 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2580894	NM_001366145.2(TRPM3):c.3397T>C (p.Ser1133Pro)	TRPM3 (S1111P +12 more)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic
Select item 2576899	NM_001366145.2(TRPM3):c.4100G>C (p.Ser1367Thr)	KLF9-DT, TRPM3 (S1192T +9 more)	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 2515734	NM_001366145.2(TRPM3):c.5026C>T (p.Arg1676Trp)	KLF9-DT, TRPM3 (R1513W +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2501854	NM_001366145.2(TRPM3):c.5123C>T (p.Thr1708Ile)	KLF9-DT, TRPM3 (T1533I +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2497710	NM_001366145.2(TRPM3):c.3541G>A (p.Glu1181Lys)	TRPM3 (E1006K +12 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2494081	NM_001366145.2(TRPM3):c.3938T>C (p.Phe1313Ser)	KLF9-DT, TRPM3 (F1160S +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488489	NM_001366145.2(TRPM3):c.4411A>G (p.Ile1471Val)	KLF9-DT, TRPM3 (I1459V +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2487115	NM_001366145.2(TRPM3):c.4943A>G (p.Asn1648Ser)	KLF9-DT, TRPM3 (N1483S +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2483331	NM_001366145.2(TRPM3):c.4862T>C (p.Ile1621Thr)	KLF9-DT, TRPM3 (I1456T +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2476528	NM_001366145.2(TRPM3):c.4071A>T (p.Lys1357Asn)	KLF9-DT, TRPM3 (K1204N +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2430061	NM_001366145.2(TRPM3):c.4685G>A (p.Cys1562Tyr)	KLF9-DT, TRPM3 (C1387Y +9 more)	Single nucleotide variant (missense variant +1 more)	Developmental disorder	GLikely benign
Select item 2428865	NM_001366145.2(TRPM3):c.4220G>A (p.Arg1407Lys)	KLF9-DT, TRPM3 (R1232K +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2399971	NM_001366145.2(TRPM3):c.5027G>A (p.Arg1676Gln)	KLF9-DT, TRPM3 (R1501Q +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2393353	NM_001366145.2(TRPM3):c.4376C>A (p.Thr1459Lys)	KLF9-DT, TRPM3 (T1294K +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2363353	NM_001366145.2(TRPM3):c.3781G>A (p.Val1261Met)	KLF9-DT, TRPM3 (V1111M +12 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2341009	NM_001366145.2(TRPM3):c.4201A>G (p.Ile1401Val)	KLF9-DT, TRPM3 (I1391V +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2338253	NM_001366145.2(TRPM3):c.4277T>C (p.Ile1426Thr)	KLF9-DT, TRPM3 (I1261T +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2336858	NM_001366145.2(TRPM3):c.4385C>T (p.Pro1462Leu)	KLF9-DT, TRPM3 (P1312L +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2330026	NM_001366145.2(TRPM3):c.4092G>T (p.Lys1364Asn)	KLF9-DT, TRPM3 (K1224N +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2294061	NM_001366145.2(TRPM3):c.4334C>T (p.Thr1445Ile)	KLF9-DT, TRPM3 (T1280I +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2290951	NM_001366145.2(TRPM3):c.4297G>A (p.Val1433Met)	KLF9-DT, TRPM3 (V1258M +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2246039	NM_001366145.2(TRPM3):c.3797C>T (p.Ala1266Val)	KLF9-DT, TRPM3 (A1101V +12 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2210054	NM_001366145.2(TRPM3):c.4068G>A (p.Met1356Ile)	KLF9-DT, TRPM3 (M1206I +9 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2119305	NC_000009.12:g.70810022T>C	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1988872	NC_000009.12:g.70809995G>A	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1975988	NC_000009.12:g.70810026T>C	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1958536	NC_000009.12:g.70810059G>A	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1904056	NC_000009.12:g.70810020C>T	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1903845	NC_000009.12:g.70810067T>C	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1900878	NC_000009.12:g.70810001T>C	MIR204, TRPM3	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 1700844	NM_001366145.2(TRPM3):c.4261G>C (p.Glu1421Gln)	TRPM3, KLF9-DT (E1246Q +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1700411	NM_001366145.2(TRPM3):c.4187C>A (p.Ala1396Asp)	KLF9-DT, TRPM3 (A1221D +9 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 1699259	NM_001366145.2(TRPM3):c.4493G>C (p.Trp1498Ser)	KLF9-DT, TRPM3 (W1323S +9 more)	Single nucleotide variant (missense variant +1 more)	Neurodevelopmental disorder	GUncertain significance
Select item 1696635	NM_001366145.2(TRPM3):c.1976A>G (p.Lys659Arg)	TRPM3 (K484R +12 more)	Single nucleotide variant (missense variant)	TRPM3-associated epilepsy syndrome	GUncertain significance

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