Annotation Detail
Information
- Associated Genes
- ERBB2
- Associated Variants
-
ERBB2 p.Tyr772_Ala775dup (p.Y772_A775dup)
(
ENST00000541774.5,
ENST00000269571.10,
ENST00000445658.6,
ENST00000406381.6,
ENST00000584450.5,
ENST00000584601.5 )
ERBB2 p.Tyr772_Ala775dup (p.Y772_A775dup) ( ENST00000269571.10, ENST00000406381.6, ENST00000445658.6, ENST00000541774.5, ENST00000584450.5, ENST00000584601.5 ) - Associated Disease
- lung adenocarcinoma
- Source Database
- ClinVar
- Description
- NM_004448.4(ERBB2):c.2314_2325dup (p.Tyr772_Ala775dup) AND Lung adenocarcinoma
- ClinVar Allele ID
- 54152
- ClinVar RefSeq Alternation Syntax
- NM_001382791.1:c.2305_2316dup
- ClinVar RefSeq Alternation Syntax
- NM_001382793.1:c.2272_2283dup
- ClinVar RefSeq Alternation Syntax
- NM_001382806.1:c.1276_1287dup
- ClinVar RefSeq Alternation Syntax
- NM_001382800.1:c.2308-317_2308-306dup
- ClinVar RefSeq Alternation Syntax
- NM_001382795.1:c.2266_2277dup
- ClinVar RefSeq Alternation Syntax
- NM_001289937.2:c.2314_2325dup
- ClinVar RefSeq Alternation Syntax
- NM_001382804.1:c.1486_1497dup
- ClinVar RefSeq Alternation Syntax
- NM_001382785.1:c.2416_2427dup
- ClinVar RefSeq Alternation Syntax
- NM_001382794.1:c.2272_2283dup
- ClinVar RefSeq Alternation Syntax
- NM_001382784.1:c.2431_2442dup
- ClinVar RefSeq Alternation Syntax
- NM_001382805.1:c.2208+1072_2208+1083dup
- ClinVar RefSeq Alternation Syntax
- NM_001382801.1:c.2266_2277dup
- ClinVar RefSeq Alternation Syntax
- NM_004448.4:c.2314_2325dup
- ClinVar RefSeq Alternation Syntax
- NM_001382790.1:c.2311_2322dup
- ClinVar RefSeq Alternation Syntax
- NM_001382796.1:c.2314_2325dup
- ClinVar RefSeq Alternation Syntax
- NM_001382803.1:c.2272_2283dup
- ClinVar RefSeq Alternation Syntax
- NM_001382783.1:c.2224_2235dup
- ClinVar RefSeq Alternation Syntax
- NM_001382802.1:c.2056_2067dup
- ClinVar RefSeq Alternation Syntax
- NR_110535.2:n.2552_2563dup
- ClinVar RefSeq Alternation Syntax
- NM_001382789.1:c.2335_2346dup
- ClinVar RefSeq Alternation Syntax
- NM_001382786.1:c.2395_2406dup
- ClinVar RefSeq Alternation Syntax
- NM_001382782.1:c.2224_2235dup
- ClinVar RefSeq Alternation Syntax
- NM_001382799.1:c.2134_2145dup
- ClinVar RefSeq Alternation Syntax
- NM_001005862.3:c.2224_2235dup
- ClinVar RefSeq Alternation Syntax
- NM_001382792.1:c.2278_2289dup
- ClinVar RefSeq Alternation Syntax
- NM_001382798.1:c.2314_2325dup
- ClinVar RefSeq Alternation Syntax
- NM_001382787.1:c.2389_2400dup
- ClinVar RefSeq Alternation Syntax
- NM_001382788.1:c.2344_2355dup
- ClinVar RefSeq Alternation Syntax
- NM_001289936.2:c.2269_2280dup
- ClinVar RefSeq Alternation Syntax
- NM_001382797.1:c.2215_2226dup
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003996361
- ClinVar Disease
- Lung adenocarcinoma
- Observed Origin Sample
- somatic
Drugs