ClinVar Genomic variation as it relates to human health
NM_003954.5(MAP3K14):c.2289A>G (p.Ala763=)
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 | |||
LOC126862575 | - | - | - | GRCh38 | - | 93 |
MAP3K14 | - | - |
GRCh38 GRCh37 |
299 | 450 | |
MAP3K14-AS1 | - | - | - | GRCh38 | - | 168 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 4, 2019 | RCV003941468.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Mar 17, 2024