Annotation Detail
Information
- Associated Genes
- ERBB2
- Associated Variants
-
ERBB2 p.Asn857Ser (p.N857S)
(
ENST00000445658.6,
ENST00000269571.10,
ENST00000584601.5,
ENST00000584450.5,
ENST00000406381.6,
ENST00000541774.5 )
ERBB2 p.Asn857Ser (p.N857S) ( ENST00000269571.10, ENST00000406381.6, ENST00000445658.6, ENST00000541774.5, ENST00000584450.5, ENST00000584601.5 ) - Associated Disease
- Neoplasm of ovary
- Source Database
- ClinVar
- Description
- NM_004448.4(ERBB2):c.2570A>G (p.Asn857Ser) AND Neoplasm of ovary
- ClinVar Allele ID
- 28919
- ClinVar RefSeq Alternation Syntax
- NM_001382790.1:c.2567A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382785.1:c.2672A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382806.1:c.1532A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382786.1:c.2651A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382784.1:c.2687A>G
- ClinVar RefSeq Alternation Syntax
- NM_001289937.2:c.2570A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382791.1:c.2561A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382802.1:c.2312A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382794.1:c.2528A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382788.1:c.2600A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382792.1:c.2534A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382793.1:c.2528A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382798.1:c.2494-202A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382795.1:c.2522A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382782.1:c.2480A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382805.1:c.2208+1465A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382799.1:c.2390A>G
- ClinVar RefSeq Alternation Syntax
- NM_001289936.2:c.2525A>G
- ClinVar RefSeq Alternation Syntax
- NM_004448.4:c.2570A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382783.1:c.2480A>G
- ClinVar RefSeq Alternation Syntax
- NR_110535.2:n.2808A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382796.1:c.2570A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382801.1:c.2446-202A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382803.1:c.2528A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382800.1:c.2384A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382804.1:c.1742A>G
- ClinVar RefSeq Alternation Syntax
- NM_001005862.3:c.2480A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382797.1:c.2471A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382787.1:c.2645A>G
- ClinVar RefSeq Alternation Syntax
- NM_001382789.1:c.2591A>G
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2004-09-30
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000014894
- ClinVar Disease
- Neoplasm of ovary
- Observed Origin Sample
- somatic
- Pubmed
- 15457249
Drugs