Annotation Detail
Information
- Associated Genes
- MYH7 LOC126861898
- Associated Variants
-
MYH7 p.Gly768Arg (p.G768R)
(
ENST00000713768.1,
ENST00000355349.4,
ENST00000713769.1 )
MYH7 p.Gly768Arg (p.G768R) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.2302G>C (p.Gly768Arg) AND not provided
- ClinVar Allele ID
- 179617
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.2302G>C
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2018-12-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000158527
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs