ClinVar Genomic variation as it relates to human health
NM_138477.4(CDAN1):c.494C>T (p.Thr165Met)
Germline
Classification
(2)
Uncertain significance
criteria provided, multiple submitters, no conflicts
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 | |||
CDAN1 | - | - |
GRCh38 GRCh37 |
568 | 642 | |
LOC130056931 | - | - | - | GRCh38 | - | 50 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Dec 21, 2022 | RCV003144739.3 | |
Uncertain significance (1) |
|
Nov 30, 2022 | RCV003481457.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 17, 2024