RNF215[gene] - ClinVar

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

Search results

Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 57132	GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3	ADORA2A, ADORA2A-AS1 +798 more	Copy number gain	See cases	GPathogenic
Select item 148861	GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3	ADORA2A, ADORA2A-AS1 +823 more	Copy number gain	See cases	GPathogenic
Select item 149114	GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3	LOC130067187, LOC130067188 +556 more	Copy number gain	See cases	GPathogenic
Select item 155348	GRCh38/hg38 22q12.1-12.2(chr22:26451042-31451926)x1	AP1B1, ASCC2 +260 more	Copy number loss	See cases	GPathogenic
Select item 57002	GRCh38/hg38 22q12.1-12.3(chr22:26979579-33992220)x3	AP1B1, ASCC2 +307 more	Copy number gain	See cases	GPathogenic
Select item 149559	GRCh38/hg38 22q12.2(chr22:30312256-30950316)x3	CCDC157, DUSP18 +54 more	Copy number gain	See cases	GUncertain significance
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)	RNF215, LOC130067210 (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
Select item 1808303	GRCh37/hg19 22q12.2(chr22:30649178-31035087)x3	CASTOR1, CCDC157 +13 more	Copy number gain	not provided	GUncertain significance
Select item 1466555	NC_000022.10:g.(?_29083885)_(34046674_?)dup	AP1B1, ASCC2 +71 more	Duplication	not provided	GUncertain significance
Select item 983188	GRCh37/hg19 22q11.1-13.33(chr22:16197005-51224252)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic
Select item 816216	GRCh37/hg19 22q12.2-13.33(chr22:30654764-51197838)x3	CERK, CHADL +271 more	Copy number gain	not provided	GPathogenic
Select item 685636	GRCh37/hg19 22q11.1-13.33(chr22:16888899-51197838)x3	TUBA8, TUBGCP6 +435 more	Copy number gain	not provided	GPathogenic
Select item 634999	inv(22)(q12.2q12.2)	NEFH, PIK3IP1 +42 more	Inversion	Anaplastic ependymoma	GLikely pathogenic
Select item 565055	GRCh37/hg19 22q11.22-12.3(chr22:22460754-35198232)x3	ADORA2A, AP1B1 +129 more	Copy number gain	not provided	GPathogenic
Select item 565022	GRCh37/hg19 22q12.2(chr22:29644625-31051719)x1	AP1B1, ASCC2 +32 more	Copy number loss	not provided	GPathogenic
Select item 442415	GRCh37/hg19 22q12.1-12.3(chr22:28349854-33013062)x3	DEPDC5, DRG1 +70 more	Copy number gain	See cases	GLikely pathogenic
Select item 441826	GRCh37/hg19 22q11.23-12.3(chr22:23637907-36614412)x3	ADORA2A, AP1B1 +131 more	Copy number gain	See cases	GPathogenic
Select item 441654	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)	ANKRD54, AP1B1 +435 more	Copy number gain	See cases	GPathogenic
Select item 441653	GRCh37/hg19 22q11.1-13.33(chr22:16888900-51197838)x3	NEFH, NF2 +435 more	Copy number gain	See cases	GPathogenic
Select item 395140	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237463)x3	ZNF280A, ZNF280B +438 more	Copy number gain	See cases	GPathogenic
Select item 394709	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51220902)x3	SMARCB1, SMC1B +438 more	Copy number gain	See cases	GPathogenic
Select item 253509	GRCh37/hg19 22q11.1-13.33(chr22:16054691-51237518)x3	A4GALT, ACO2 +438 more	Copy number gain	See cases	GPathogenic

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: 52