RGD:13522475 Rat Genome Database

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Variant: RGD:13522475 -  Homo sapiens

RGD ID: 13522475
RS ID: rs71446397
ClinVar ID: CV492889
Genic Status: GENIC
Type: deletion (SO:0000159) 
Associated Genes: SLC10A1  
Reference Nucleotide: C
Variant Nucleotide: -
Position
Assembly Chr Position
GRCh37 14 70,245,894
GRCh38 14 69,779,177
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_003049.4:c.746+5del
NC_000014.9:g.69779178del
NC_000014.8:g.70245895del
 08/22/2018 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC10A1
Accession:NM_003049
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000591784 CLINVAR
dbSNP (RS) rs71446397 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene SLC10A1 CLINVAR
OMIM 182396 CLINVAR