Annotation Detail
Information
- Associated Genes
- MYH7
- Associated Variants
-
MYH7 p.Arg1045Leu (p.R1045L)
(
ENST00000713769.1,
ENST00000713768.1,
ENST00000355349.4 )
MYH7 p.Arg1045Leu (p.R1045L) ( ENST00000355349.4, ENST00000713768.1, ENST00000713769.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000257.4(MYH7):c.3134G>T (p.Arg1045Leu) AND not provided
- ClinVar Allele ID
- 52118
- ClinVar RefSeq Alternation Syntax
- NM_000257.4:c.3134G>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2022-10-12
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001703459
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs