ClinVar Genomic variation as it relates to human health
NM_002467.6(MYC):c.217A>G (p.Thr73Ala)
Germline
Classification
(1)
Pathogenic
criteria provided, single submitter
Somatic
No data submitted for somatic clinical impact
Somatic
Oncogenicity
(1)
Oncogenic
no assertion criteria provided
Genes
Gene | OMIM | ClinGen Gene Dosage Sensitivity Curation | Variation Viewer | Related variants | ||
---|---|---|---|---|---|---|
HI score | TS score | Within gene | All | |||
MYC | - | - |
GRCh38 GRCh37 |
33 | 86 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Pathogenic (1) |
|
Jul 1, 2023 | RCV003440642.8 |
Citations for germline classification of this variant
HelpConditions - Somatic
Tumor type | Clinical impact (# of submissions) | Oncogenicity | Last evaluated | Variation/condition record |
---|---|---|---|---|
|
Oncogenic
|
Jan 24, 2024 | RCV003883217.1 |
Citations for somatic classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 04, 2024