RGD:28907751 Rat Genome Database

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Variant: RGD:28907751 -  Homo sapiens

RGD ID: 28907751
RS ID: rs2037637000
ClinVar ID: CV866740
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABCC2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 101,542,513
GRCh38 10 99,782,756
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1208t1:c.-89G>A
NM_000392.5:c.-89G>A
LRG_1208:g.5159G>A
NG_011798.2:g.5159G>A
More... 		01/12/2018 5 prime utr variant uncertain significance Hyperbilirubinemia type 2; HYPERBILIRUBINEMIA, DUBIN-JOHNSON TYPE; Jaundice, Chronic Idiopathic
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ABCC2
Accession:NM_000392
Location:5UTRS;EXON

Gene Symbol:ABCC2
Accession:XM_011539291
Location:5UTRS;EXON

Gene Symbol:ABCC2
Accession:XM_006717631
Location:5UTRS;EXON

Gene Symbol:ABCC2
Accession:XM_017015675
Location:5UTRS;EXON

Gene Symbol:ABCC2
Accession:XM_047424598
Location:5UTRS;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 RCV001107400 CLINVAR
dbSNP (RS) rs2037637000 CLINVAR
MedGen C0022350 CLINVAR
NCBI Gene ABCC2 CLINVAR
OMIM 237500 CLINVAR
  601107 CLINVAR
SNOMED CT 44553005 CLINVAR