RGD:13484408 Rat Genome Database

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Variant: RGD:13484408 -  Homo sapiens

RGD ID: 13484408
RS ID: rs768374617
ClinVar ID: CV457124
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HNRNPA2B1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 26,235,457
GRCh38 7 26,195,837
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.13:g.26235457G>A
NG_029680.1:g.9957C>T
NM_031243.2:c.757+10C>T
NC_000007.14:g.26195837G>A
More... 		06/09/2018 intron variant likely benign MULTISYSTEM PROTEINOPATHY 2

Variant Details
Variant Transcripts
Gene Symbol:HNRNPA2B1
Accession:XM_017012109
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420303
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420302
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420298
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:NM_002137
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_005249729
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420301
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420299
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420305
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420300
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420304
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_047420306
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:NM_031243
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XM_017012110
Location:INTRON

Gene Symbol:HNRNPA2B1
Accession:XR_242077
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_242076
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744673
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744674
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744672
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060012
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_428077
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744670
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744665
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744671
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_001744666
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_002956424
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060015
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060014
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060013
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060011
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060017
Location:INTRON;NON-CODING

Gene Symbol:HNRNPA2B1
Accession:XR_007060016
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001430458 CLINVAR
dbSNP (RS) rs768374617 CLINVAR
MedGen C3809468 CLINVAR
NCBI Gene HNRNPA2B1 CLINVAR
OMIM 600124 CLINVAR
  615422 CLINVAR