RGD:13435949 Rat Genome Database

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Variant: RGD:13435949 -  Homo sapiens

RGD ID: 13435949
RS ID: rs765563255
ClinVar ID: CV432868
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HBA1  LOC106804613  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 227,263
GRCh38 16 177,264
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000016.10:g.177264G>A
NC_000016.9:g.227263G>A
NM_000558.3:c.301-19G>A
NM_000558.5:c.301-19G>A
More... 		07/05/2017 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:HBA1
Accession:NM_000558
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:26467025  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003478076 CLINVAR
dbSNP (RS) rs765563255 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene 106804613 CLINVAR
  HBA1 CLINVAR
OMIM 141800 CLINVAR