RGD:9693003 Rat Genome Database

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Variant: RGD:9693003 -  Homo sapiens

RGD ID: 9693003
RS ID: rs727503970
ClinVar ID: CV177783
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IVD  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 15 40,707,068
GRCh38 15 40,414,869
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000015.10:g.40414869A>G
NC_000015.9:g.40707068A>G
NG_011986.2:g.14385A>G
NM_001354601.3:c.785-20A>G
More... 		01/22/2014 intron variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:IVD
Accession:XM_017022158
Location:EXON

Gene Symbol:IVD
Accession:XM_006720495
Location:INTRON

Gene Symbol:IVD
Accession:NM_001354597
Location:INTRON

Gene Symbol:IVD
Accession:XM_047432461
Location:INTRON

Gene Symbol:IVD
Accession:XM_047432462
Location:INTRON

Gene Symbol:IVD
Accession:XM_017022157
Location:INTRON

Gene Symbol:IVD
Accession:NM_001354600
Location:INTRON

Gene Symbol:IVD
Accession:XM_047432463
Location:INTRON

Gene Symbol:IVD
Accession:XM_017022149
Location:INTRON

Gene Symbol:IVD
Accession:NM_001354601
Location:INTRON

Gene Symbol:IVD
Accession:XM_017022155
Location:INTRON

Gene Symbol:IVD
Accession:XM_017022154
Location:INTRON

Gene Symbol:IVD
Accession:NM_001354599
Location:INTRON

Gene Symbol:IVD
Accession:XM_047432464
Location:INTRON

Gene Symbol:IVD
Accession:NM_001159508
Location:INTRON

Gene Symbol:IVD
Accession:NM_002225
Location:INTRON

Gene Symbol:IVD
Accession:XM_017022153
Location:INTRON

Gene Symbol:IVD
Accession:NM_001354598
Location:INTRON

Gene Symbol:IVD
Accession:XM_047432460
Location:INTRON

Gene Symbol:IVD
Accession:XR_007064441
Location:INTRON;NON-CODING

Gene Symbol:IVD
Accession:XR_007064442
Location:INTRON;NON-CODING

Gene Symbol:IVD
Accession:NR_148925
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000153386 CLINVAR
dbSNP (RS) rs727503970 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene IVD CLINVAR
OMIM 607036 CLINVAR