Annotation Detail

Information
Associated Genes
HBB LOC107133510 LOC110006319
Associated Variants
HBB p.Val110Leu (p.V110L) ( ENST00000335295.4, ENST00000647020.1 )
HBB p.Val110Leu (p.V110L) ( ENST00000335295.4, ENST00000647020.1 )
Source Database
ClinVar
Description
NM_000518.5(HBB):c.328G>C (p.Val110Leu) AND HEMOGLOBIN JOHNSTOWN
ClinVar Allele ID
30269
ClinVar RefSeq Alternation Syntax
NM_000518.5:c.328G>C
Clinical Significance Description
other
Clinical Significance Last Update
2017-12-12
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000016428
Observed Origin Sample
germline
Pubmed
15658189
Pubmed
2272838
Drugs