ClinVar Genomic variation as it relates to human health
NM_000077.5(CDKN2A):c.226_244del (p.Ala76fs)
Germline
Classification
(2)
Pathogenic; risk factor
no assertion criteria provided
Somatic
No data submitted for somatic clinical impact
Somatic
No data submitted for oncogenicity
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
CDKN2A | Sufficient evidence for dosage pathogenicity | No evidence available |
GRCh38 GRCh37 |
1260 | 1412 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
risk factor (1) |
|
Jun 1, 2012 | RCV000010013.6 | |
Pathogenic (1) |
|
Jun 1, 2012 | RCV000010015.7 |
Citations for germline classification of this variant
HelpText-mined citations for rs587776716 ...
HelpThese citations are identified by LitVar using
the rs number, so they may include citations for more than one variant
at this location. Please review the LitVar results carefully for your
variant of interest.
Record last updated Sep 17, 2022
NCBI staff reviewed the sequence information reported in PubMed 7670475 Fig. 3 to determine the location of this allele on the current reference sequence.