ClinVar Genomic variation as it relates to human health
NM_144638.3(TMEM42):c.17G>A (p.Gly6Glu)
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 | |||
KIF15 | - | - |
GRCh38 GRCh38 GRCh37 |
99 | 125 | |
LOC129936609 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
MIR564 | - | - | - |
GRCh38 GRCh38 |
- | 5 |
TMEM42 | - | - | - |
GRCh38 GRCh38 GRCh37 |
- | 26 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Uncertain significance (1) |
|
Aug 30, 2021 | RCV004096419.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 18, 2024