"Ambry Genetics"[submitter] AND "RNF215"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2374894	NM_001017981.2(RNF215):c.1117C>T (p.Arg373Cys)	RNF215 (R373C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550584	NM_001017981.2(RNF215):c.1091T>C (p.Leu364Pro)	RNF215 (L364P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2459400	NM_001017981.2(RNF215):c.1018G>T (p.Val340Leu)	RNF215 (V340L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155307	NM_001017981.2(RNF215):c.941C>T (p.Ala314Val)	RNF215 (A314V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366460	NM_001017981.2(RNF215):c.926G>A (p.Arg309Gln)	RNF215 (R309Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279715	NM_001017981.2(RNF215):c.917G>A (p.Arg306Gln)	RNF215 (R306Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323671	NM_001017981.2(RNF215):c.848G>A (p.Arg283Gln)	RNF215 (R283Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2254943	NM_001017981.2(RNF215):c.842G>A (p.Ser281Asn)	RNF215 (S281N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210819	NM_001017981.2(RNF215):c.824G>A (p.Arg275Gln)	RNF215 (R275Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314851	NM_001017981.2(RNF215):c.805C>T (p.Leu269Phe)	RNF215 (L269F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155306	NM_001017981.2(RNF215):c.731G>A (p.Arg244His)	RNF215 (R244H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477647	NM_001017981.2(RNF215):c.730C>T (p.Arg244Cys)	RNF215 (R244C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2593295	NM_001017981.2(RNF215):c.713T>A (p.Val238Asp)	RNF215 (V238D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274278	NM_001017981.2(RNF215):c.455C>T (p.Ala152Val)	RNF215 (A152V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517496	NM_001017981.2(RNF215):c.437G>A (p.Arg146Gln)	RNF215 (R146Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598500	NM_001017981.2(RNF215):c.434G>A (p.Arg145Gln)	RNF215 (R145Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350223	NM_001017981.2(RNF215):c.398C>T (p.Pro133Leu)	RNF215 (P133L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546722	NM_001017981.2(RNF215):c.325G>A (p.Gly109Ser)	RNF215 (G109S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326278	NM_001017981.2(RNF215):c.275G>T (p.Arg92Leu)	RNF215 (R92L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155304	NM_001017981.2(RNF215):c.274C>G (p.Arg92Gly)	RNF215 (R92G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470355	NM_001017981.2(RNF215):c.260C>G (p.Pro87Arg)	RNF215 (P87R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314852	NM_001017981.2(RNF215):c.254C>G (p.Pro85Arg)	RNF215 (P85R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3314850	NM_001017981.2(RNF215):c.155C>T (p.Ala52Val)	LOC130067210, RNF215 (A52V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509201	NM_001017981.2(RNF215):c.146C>T (p.Ala49Val)	LOC130067210, RNF215 (A49V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345892	NM_001017981.2(RNF215):c.136A>T (p.Ser46Cys)	LOC130067210, RNF215 (S46C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396939	NM_001017981.2(RNF215):c.131A>C (p.Asp44Ala)	LOC130067210, RNF215 (D44A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3155303	NM_001017981.2(RNF215):c.128C>T (p.Ala43Val)	LOC130067210, RNF215 (A43V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395086	NM_001017981.2(RNF215):c.124G>C (p.Ala42Pro)	LOC130067210, RNF215 (A42P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235722	NM_001017981.2(RNF215):c.107T>A (p.Leu36Gln)	LOC130067210, RNF215 (L36Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 29