RGD:8575448 Rat Genome Database

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Variant: RGD:8575448 -  Homo sapiens

RGD ID: 8575448
ClinVar ID: CV109795
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNT2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 196,295,718
GRCh38 1 196,326,588
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.196326588A>G
NC_000001.10:g.196295718A>G
NM_001287819.1:c.2276+129T>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNT2
Accession:XM_017001180
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_017001183
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_017001185
Location:INTRON

Gene Symbol:KCNT2
Accession:NM_001287819
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_017001179
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_006711294
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_006711295
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_011509483
Location:INTRON

Gene Symbol:KCNT2
Accession:NM_198503
Location:INTRON

Gene Symbol:KCNT2
Accession:XM_017001181
Location:INTRON

Gene Symbol:KCNT2
Accession:NM_001287820
Location:INTRON

Gene Symbol:KCNT2
Accession:XR_001737149
Location:INTRON;NON-CODING

Gene Symbol:KCNT2
Accession:NR_146057
Location:INTRON;NON-CODING

Gene Symbol:KCNT2
Accession:XR_001737151
Location:INTRON;NON-CODING

Gene Symbol:KCNT2
Accession:NR_146058
Location:INTRON;NON-CODING

Variant Samples