Related gene-specific medical variations for Gene (Select 6875) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3452685	NM_005640.3(TAF4B):c.73A>T (p.Met25Leu)	LOC130062319, TAF4B (M25L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3324265	NM_005640.3(TAF4B):c.17C>T (p.Thr6Ile)	LOC130062319, TAF4B (T6I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512637	NM_005640.3(TAF4B):c.47C>T (p.Ala16Val)	LOC130062319, TAF4B (A16V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337402	NM_005640.3(TAF4B):c.128G>A (p.Gly43Asp)	LOC130062319, TAF4B (G43D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304453	NM_005640.3(TAF4B):c.106G>A (p.Glu36Lys)	LOC130062319, TAF4B (E36K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 786339	NM_005640.3(TAF4B):c.147T>C (p.Pro49=)	LOC130062319, TAF4B	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 778769	NM_005640.3(TAF4B):c.130G>C (p.Ala44Pro)	LOC130062319, TAF4B (A44P)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign

ClinVar