RGD:150445162 Rat Genome Database

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Variant: RGD:150445162 -  Homo sapiens

RGD ID: 150445162
RS ID: rs45581440
ClinVar ID: CV1261153
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ABCB4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 87,047,588
GRCh38 7 87,418,272
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.87047588T>C
NM_000443.4:c.2478+265A>G
NC_000007.14:g.87418272T>C
NG_007118.2:g.67161A>G
More... 		06/18/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ABCB4
Accession:XM_047420476
Location:INTRON

Gene Symbol:ABCB4
Accession:NM_018849
Location:INTRON

Gene Symbol:ABCB4
Accession:NM_000443
Location:INTRON

Gene Symbol:ABCB4
Accession:XM_011516309
Location:INTRON

Gene Symbol:ABCB4
Accession:NM_018850
Location:INTRON

Gene Symbol:ABCB4
Accession:XM_047420477
Location:INTRON

Gene Symbol:ABCB4
Accession:XM_011516308
Location:INTRON

Gene Symbol:ABCB4
Accession:XM_047420475
Location:INTRON

Gene Symbol:ABCB4
Accession:XR_007060046
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060045
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060050
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060049
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060048
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_001744810
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060052
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060053
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060047
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060054
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060055
Location:INTRON;NON-CODING

Gene Symbol:ABCB4
Accession:XR_007060051
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001679827 CLINVAR
dbSNP (RS) rs45581440 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ABCB4 CLINVAR
OMIM 171060 CLINVAR