RGD:8628788 Rat Genome Database

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Variant: RGD:8628788 -  Homo sapiens

RGD ID: 8628788
ClinVar ID: CV83932
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNC4  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 110,768,931
GRCh38 1 110,226,309
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001039574.2:c.1819+131C>T
NM_004978.4:c.1819+131C>T
NC_000001.11:g.110226309C>T
NC_000001.10:g.110768931C>T
More... 		intron|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNC4
Accession:XM_047419680
Location:INTRON

Gene Symbol:KCNC4
Accession:XM_047419679
Location:INTRON

Gene Symbol:KCNC4
Accession:XM_006710625
Location:INTRON

Gene Symbol:KCNC4
Accession:NM_001039574
Location:INTRON

Gene Symbol:KCNC4
Accession:XM_024446790
Location:INTRON

Gene Symbol:KCNC4
Accession:NM_004978
Location:INTRON

Gene Symbol:KCNC4
Accession:XM_011541401
Location:INTRON

Gene Symbol:KCNC4
Accession:NM_001377330
Location:INTRON

Gene Symbol:KCNC4
Accession:XM_011541404
Location:INTRON

Gene Symbol:KCNC4
Accession:NM_001377331
Location:INTRON

Gene Symbol:KCNC4
Accession:NR_036437
Location:INTRON;NON-CODING

Variant Samples