RGD:405028817 Rat Genome Database

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Variant: RGD:405028817 -  Homo sapiens

RGD ID: 405028817
ClinVar ID: CV2967901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCND2  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 120,372,941
GRCh38 7 120,732,887
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.1116-16T>G
NG_034230.1:g.464220T>G
NC_000007.14:g.120732887T>G
NC_000007.13:g.120372941T>G
 05/31/2023 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:KCND2
Accession:NM_012281
Location:INTRON

Gene Symbol:KCND2
Accession:XM_047420346
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003601474 CLINVAR
MedGen C0270855 CLINVAR
NCBI Gene KCND2 CLINVAR
OMIM 605410 CLINVAR
SNOMED CT 44423001 CLINVAR