RGD:150496766 Rat Genome Database

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Variant: RGD:150496766 -  Homo sapiens

RGD ID: 150496766
RS ID: rs12728253
ClinVar ID: CV1283409
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCND3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 112,531,507
GRCh38 1 111,988,885
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004980.5:c.-210G>T
NM_172198.3:c.-210G>T
NM_001378969.1:c.-73+620G>T
NM_001378970.1:c.-73+620G>T
More... 		06/23/2018 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KCND3
Accession:NM_172198
Location:5UTRS;EXON

Gene Symbol:KCND3
Accession:NM_004980
Location:5UTRS;EXON

Gene Symbol:KCND3
Accession:XM_006710629
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_006710632
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_011541427
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_011541428
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_011541426
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_011541425
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_017001244
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:XM_017001245
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:NM_001378970
Location:5UTRS;INTRON

Gene Symbol:KCND3
Accession:NM_001378969
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001717734 CLINVAR
dbSNP (RS) rs12728253 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCND3 CLINVAR
OMIM 605411 CLINVAR