ClinVar Genomic variation as it relates to human health
NM_001379228.1(MRAP):c.180G>A (p.Met60Ile)
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 | |||
LOC125418060 | - | - | - | GRCh38 | - | 45 |
MRAP | - | - |
GRCh38 GRCh37 |
20 | 120 | |
MRAP-AS1 | - | - | - | GRCh38 | - | 45 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Feb 3, 2023 | RCV003186339.2 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated May 01, 2024