Related gene-specific medical variations for Gene (Select 135932) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3178797	NM_001282876.2(TMEM139):c.147C>G (p.Phe49Leu)	LOC126860210, TMEM139 +1 more (F49L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2658110	NM_001282876.2(TMEM139):c.245G>A (p.Arg82Gln)	TMEM139, TMEM139-AS1 (R82Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2610908	NM_001282876.2(TMEM139):c.183G>C (p.Trp61Cys)	LOC126860210, TMEM139 +1 more (W61C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2508453	NM_001282876.2(TMEM139):c.98C>T (p.Thr33Met)	LOC126860210, TMEM139 +1 more (T33M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2482231	NM_001282876.2(TMEM139):c.194C>G (p.Ser65Cys)	LOC126860210, TMEM139 +1 more (S65C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2322373	NM_001282876.2(TMEM139):c.38C>T (p.Pro13Leu)	LOC126860210, TMEM139 +1 more (P13L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2318193	NM_001282876.2(TMEM139):c.223C>G (p.Pro75Ala)	LOC126860210, TMEM139 +1 more (P75A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

ClinVar