ClinVar Genomic variation as it relates to human health
NM_001372106.1(DNAH10):c.12288T>A (p.Ile4096=)
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 | |||
DNAH10 | - | - |
GRCh38 GRCh38 GRCh37 |
435 | 544 | |
DNAH10OS | - | - | - |
GRCh38 GRCh38 |
- | 82 |
Conditions - Germline
Condition | Classification
(# of submissions) |
Review status | Last evaluated | Variation/condition record |
---|---|---|---|---|
Likely benign (1) |
|
Apr 1, 2023 | RCV003398232.9 |
Citations for germline classification of this variant
HelpText-mined citations for this variant ...
HelpRecord last updated Oct 08, 2024