RGD:150436472 Rat Genome Database

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Variant: RGD:150436472 -  Homo sapiens

RGD ID: 150436472
RS ID: rs181685823
ClinVar ID: CV1270965
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCND2  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 119,913,490
GRCh38 7 120,273,436
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_012281.3:c.-1197A>C
NC_000007.14:g.120273436A>C
NC_000007.13:g.119913490A>C
NG_034230.1:g.4769A>C
 05/12/2021 5 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:KCND2
Accession:NM_012281
Location:5UTRS;EXON

Gene Symbol:KCND2
Accession:XM_047420346
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001689515 CLINVAR
dbSNP (RS) rs181685823 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCND2 CLINVAR
OMIM 605410 CLINVAR