RGD:150452216 Rat Genome Database

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Variant: RGD:150452216 -  Homo sapiens

RGD ID: 150452216
RS ID: rs76007712
ClinVar ID: CV1276700
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNRNPA1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 54,676,748
GRCh38 12 54,282,964
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002136.4:c.751+90A>G
NM_031157.4:c.751+90A>G
NG_033830.1:g.7261A>G
NC_000012.12:g.54282964A>G
More... 		05/12/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:HNRNPA1
Accession:NM_031157
Location:INTRON

Gene Symbol:HNRNPA1
Accession:NM_002136
Location:INTRON

Gene Symbol:HNRNPA1
Accession:NR_135167
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001708489 CLINVAR
dbSNP (RS) rs76007712 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene HNRNPA1 CLINVAR
OMIM 164017 CLINVAR