ClinVar Genomic variation as it relates to human health
NM_012454.4(TIAM2):c.4150A>G (p.Thr1384Ala)
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 | |||
TFB1M | - | - |
GRCh38 GRCh37 |
17 | 104 | |
TIAM2 | - | - |
GRCh38 GRCh37 |
89 | 161 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Mar 31, 2023 | RCV004305768.1 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Aug 18, 2024