RGD:15157685 Rat Genome Database

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Variant: RGD:15157685 -  Homo sapiens

RGD ID: 15157685
RS ID: rs79307098
ClinVar ID: CV730542
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNK9  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 8 140,631,352
GRCh38 8 139,619,109
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282534.2:c.284-10C>G
NG_012842.3:g.88948C>G
NC_000008.11:g.139619109G>C
NC_000008.10:g.140631352G>C
More... 		04/03/2018 intron variant benign none provided

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

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

Variant Samples
Additional References at PubMed
PMID:25741868   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000880865 CLINVAR
  RCV003920521 CLINVAR
dbSNP (RS) rs79307098 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KCNK9 CLINVAR
OMIM 605874 CLINVAR