RGD:8634623 Rat Genome Database

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Variant: RGD:8634623 -  Homo sapiens

RGD ID: 8634623
ClinVar ID: CV89843
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLCO1A2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 21,467,616
GRCh38 12 21,314,682
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_021094.3:c.203-1G>A
NM_134431.3:c.203-1G>A
NC_000012.12:g.21314682C>T
NC_000012.11:g.21467616C>T
More... 		splice-3|splice acceptor variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:SLCO1A2
Accession:NM_001386962
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386953
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386919
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386937
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386922
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386890
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386908
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386920
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386929
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386938
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386963
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386940
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386927
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386939
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386931
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386961
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386954
Location:5UTRS;INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386882
Location:INTRON

Gene Symbol:SLCO1A2
Accession:XM_011520819
Location:INTRON

Gene Symbol:SLCO1A2
Accession:XM_024449138
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386887
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386951
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386886
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386879
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386949
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_134431
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_021094
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386960
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386947
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386926
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386946
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386880
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386958
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386921
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386952
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386881
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386959
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386878
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NM_001386948
Location:INTRON

Gene Symbol:SLCO1A2
Accession:NR_170341
Location:INTRON;NON-CODING

Gene Symbol:SLCO1A2
Accession:NR_170343
Location:INTRON;NON-CODING

Gene Symbol:SLCO1A2
Accession:NR_170340
Location:INTRON;NON-CODING

Variant Samples