Related gene-specific medical variations for Gene (Select 56) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3139289	NM_001612.6(ACRV1):c.668T>C (p.Phe223Ser)	ACRV1, CHEK1 (F153S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3139278	NM_001612.6(ACRV1):c.176C>G (p.Ser59Cys)	ACRV1, CHEK1 (S59C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607272	NM_001612.6(ACRV1):c.76C>A (p.Leu26Ile)	ACRV1, CHEK1 (L26I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557071	NM_001612.6(ACRV1):c.611G>A (p.Arg204His)	ACRV1, CHEK1 (R149H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493441	NM_001612.6(ACRV1):c.794T>C (p.Ile265Thr)	ACRV1, CHEK1 (I210T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321970	NM_001612.6(ACRV1):c.370C>T (p.Leu124Phe)	ACRV1, CHEK1 (L69F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269339	NM_001612.6(ACRV1):c.229A>C (p.Lys77Gln)	ACRV1, CHEK1 (K77Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161729	NM_001612.6(ACRV1):c.623C>T (p.Thr208Ile)	ACRV1, CHEK1 (T138I +3 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

ClinVar