ClinVar Genomic variation as it relates to human health
NM_017762.3(MTMR10):c.1763C>G (p.Pro588Arg)
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 | |||
FAN1 | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
172 | 569 | |
MTMR10 | - | - | - |
GRCh38 GRCh38 GRCh38 GRCh37 |
23 | 421 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Sep 26, 2023 | RCV004509553.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Sep 01, 2024