RGD:8654229 Rat Genome Database

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Variant: RGD:8654229 -  Homo sapiens

RGD ID: 8654229
ClinVar ID: CV130804
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNC2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 75,464,840
GRCh38 12 75,071,060
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.75071060G>T
NC_000012.11:g.75464840G>T
NM_001260497.1:c.688-19743C>A
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNC2
Accession:NM_153748
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_139137
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414197
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414192
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428817
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428816
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414193
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414195
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001260498
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001260497
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428813
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_139136
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001260499
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414202
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414206
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_006719383
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428811
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414199
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414198
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414213
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_006719390
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428818
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428810
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414196
Location:INTRON

Gene Symbol:KCNC2
Accession:NM_001414194
Location:INTRON

Gene Symbol:KCNC2
Accession:XM_047428812
Location:INTRON

Gene Symbol:KCNC2
Accession:NR_182259
Location:INTRON;NON-CODING

Gene Symbol:KCNC2
Accession:NR_182257
Location:INTRON;NON-CODING

Variant Samples