RGD:13833237 Rat Genome Database

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Variant: RGD:13833237 -  Homo sapiens

RGD ID: 13833237
RS ID: rs145427140
ClinVar ID: CV584466
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABCC2  LOC108281165  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 10 101,544,537
GRCh38 10 99,784,780
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1208t1:c.206A>C
NM_000392.5:c.206A>C
LRG_1208:g.7183A>C
NG_011798.2:g.7183A>C
More... 		07/24/2017 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:ABCC2
Accession:XM_011539291
Location:EXON

Gene Symbol:ABCC2
Accession:XM_047424598
Location:EXON

Gene Symbol:ABCC2
Accession:NM_000392
Location:EXON

Gene Symbol:ABCC2
Accession:XM_017015675
Location:EXON

Gene Symbol:ABCC2
Accession:XM_006717631
Location:EXON

Gene Symbol:ABCC2
Accession:XR_945604
Location:EXON;NON-CODING

Gene Symbol:ABCC2
Accession:XM_006717630
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000728428 CLINVAR
dbSNP (RS) rs145427140 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ABCC2 CLINVAR
  LOC108281165 CLINVAR
OMIM 601107 CLINVAR