"Ambry Genetics"[submitter] AND "TMEM170A"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2298451	NM_145254.3(TMEM170A):c.416G>C (p.Arg139Pro)	TMEM170A (R71P +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2334341	NM_145254.3(TMEM170A):c.230A>G (p.Lys77Arg)	TMEM170A (K77R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2532028	NM_145254.3(TMEM170A):c.175C>G (p.Leu59Val)	TMEM170A (L21V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2230252	NM_145254.3(TMEM170A):c.103C>G (p.Pro35Ala)	TMEM170A (P35A)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2349185	NM_145254.3(TMEM170A):c.97C>G (p.Leu33Val)	TMEM170A (L33V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2381213	NM_145254.3(TMEM170A):c.91G>A (p.Gly31Arg)	TMEM170A (G31R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2481828	NM_145254.3(TMEM170A):c.7C>T (p.Arg3Cys)	TMEM170A (R3C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

ClinVar