TEX36[gene] and "single gene"[properties] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2318827	NM_001128202.3(TEX36):c.554A>T (p.Glu185Val)	TEX36 (E185V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2618371	NM_001128202.3(TEX36):c.433C>G (p.Arg145Gly)	TEX36 (R145G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622277	NM_001128202.3(TEX36):c.314G>T (p.Arg105Ile)	TEX36 (R105I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3325576	NM_001128202.3(TEX36):c.305A>G (p.His102Arg)	TEX36 (H102R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3176404	NM_001128202.3(TEX36):c.304C>T (p.His102Tyr)	TEX36 (H102Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208383	NM_001128202.3(TEX36):c.274C>T (p.Arg92Cys)	TEX36 (R92C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353632	NM_001128202.3(TEX36):c.25C>A (p.Pro9Thr)	TEX36 (P9T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar