ClinVar Genomic variation as it relates to human health
NM_000136.3(FANCC):c.546C>A (p.Ser182=)
Germline
Classification
(1)
Likely benign
criteria provided, single submitter
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 | |||
AOPEP | - | - |
GRCh38 GRCh37 |
24 | 1375 | |
FANCC | - | - |
GRCh38 GRCh37 |
655 | 2012 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Jun 20, 2022 | RCV002349761.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 01, 2024