Related gene-specific medical variations for Gene (Select 9473) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3456171	NM_001105556.3(THEMIS2):c.7C>T (p.Pro3Ser)	LOC129929908, THEMIS2 (P3S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3456169	NM_001105556.3(THEMIS2):c.1168G>A (p.Val390Met)	LOC129929909, THEMIS2 (V390M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3456167	NM_001105556.3(THEMIS2):c.1189C>T (p.Arg397Trp)	LOC129929909, THEMIS2 (R201W +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3456166	NM_001105556.3(THEMIS2):c.1138G>A (p.Gly380Ser)	LOC129929909, THEMIS2 (G380S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3177052	NM_001105556.3(THEMIS2):c.8C>T (p.Pro3Leu)	LOC129929908, THEMIS2 (P3L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2428643	NM_001105556.3(THEMIS2):c.980G>A (p.Arg327Gln)	THEMIS2 (R327Q)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2211657	NM_001105556.3(THEMIS2):c.1202A>G (p.Gln401Arg)	LOC129929909, THEMIS2 (Q205R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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