ClinVar Genomic variation as it relates to human health
NM_198688.3(KRTAP10-6):c.740C>T (p.Ser247Phe)
Germline
Classification
(1)
Uncertain significance
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 | |||
KRTAP10-6 | - | - | - |
GRCh38 GRCh37 |
- | 131 |
TSPEAR | - | - |
GRCh38 GRCh37 |
409 | 1007 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
May 31, 2023 | RCV004293311.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 17, 2024