Annotation Detail
Information
- Associated Genes
- LY9
- Associated Variants
-
LY9 p.Met602Val (p.M602V)
(
ENST00000263285.11,
ENST00000392203.8,
ENST00000368037.9 )
LY9 p.Met602Val (p.M602V) ( ENST00000263285.11, ENST00000368037.9, ENST00000392203.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_002348.4(LY9):c.1804A>G (p.Met602Val) AND not provided
- ClinVar Allele ID
- 1230885
- ClinVar RefSeq Alternation Syntax
- NM_001261457.2:c.1534A>G
- ClinVar RefSeq Alternation Syntax
- NM_001261456.2:c.1762A>G
- ClinVar RefSeq Alternation Syntax
- NM_002348.4:c.1804A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2020-02-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001641434
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs