RGD:8650135 Rat Genome Database

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Variant: RGD:8650135 -  Homo sapiens

RGD ID: 8650135
ClinVar ID: CV126709
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNK9  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 140,660,083
GRCh38 8 139,647,840
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282534.1:c.284-28741C>G
NG_012842.2:g.60217C>G
NC_000008.11:g.139647840G>C
NC_000008.10:g.140660083G>C
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNK9
Accession:NM_001282534
Location:INTRON

Gene Symbol:KCNK9
Accession:NR_104210
Location:INTRON;NON-CODING

Variant Samples