"Ambry Genetics"[submitter] AND "CRIP2"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2611731	NM_001312.4(CRIP2):c.158G>A (p.Cys53Tyr)	CRIP2 (C127Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2252524	NM_001312.4(CRIP2):c.221C>T (p.Ser74Phe)	CRIP2 (S148F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2610793	NM_001312.4(CRIP2):c.241C>A (p.Leu81Met)	CRIP2 (L81M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077453	NM_001312.4(CRIP2):c.254C>A (p.Pro85Gln)	CRIP2 (P159Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2291851	NM_001312.4(CRIP2):c.258G>C (p.Gln86His)	CRIP2 (Q160H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2235766	NM_001312.4(CRIP2):c.266G>A (p.Gly89Asp)	CRIP2 (G89D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2599607	NM_001312.4(CRIP2):c.287C>G (p.Ala96Gly)	CRIP2 (A96G +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2607899	NM_001312.4(CRIP2):c.290G>A (p.Arg97Gln)	CRIP2 (R171Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2478527	NM_001312.4(CRIP2):c.298G>A (p.Glu100Lys)	CRIP2 (E100K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2596223	NM_001312.4(CRIP2):c.312C>A (p.Ser104Arg)	CRIP2 (S178R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2297514	NM_001312.4(CRIP2):c.331A>C (p.Ser111Arg)	CRIP2 (S185R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2347283	NM_001312.4(CRIP2):c.383G>A (p.Arg128His)	CRIP2 (R202H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2542847	NM_001312.4(CRIP2):c.405C>A (p.Phe135Leu)	CRIP2 (F135L +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3077454	NM_001312.4(CRIP2):c.496G>A (p.Ala166Thr)	CRIP2 (A240T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3077455	NM_001312.4(CRIP2):c.528G>C (p.Lys176Asn)	CRIP2 (K176N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance