Annotation Detail

Information
Associated Genes
HBB LOC107133510 LOC110006319
Associated Variants
HBB p.Cys113Arg (p.C113R) ( ENST00000335295.4, ENST00000647020.1 )
HBB p.Cys113Arg (p.C113R) ( ENST00000335295.4, ENST00000647020.1 )
Source Database
ClinVar
Description
NM_000518.5(HBB):c.337T>C (p.Cys113Arg) AND HEMOGLOBIN INDIANAPOLIS
ClinVar Allele ID
30246
ClinVar RefSeq Alternation Syntax
NM_000518.5:c.337T>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/RCV000016392
Observed Origin Sample
germline
Pubmed
2005117
Pubmed
721609
Pubmed
3781865
Pubmed
5698750
Drugs