RGD:150469284 Rat Genome Database

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Variant: RGD:150469284 -  Homo sapiens

RGD ID: 150469284
RS ID: rs869704
ClinVar ID: CV1219048
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCNKB  LOC106501713  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 16,374,185
GRCh38 1 16,047,690
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000085.5:c.359-215G>A
NG_042865.1:g.3198G>A
NC_000001.11:g.16047690G>A
NC_000001.10:g.16374185G>A
More... 		11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CLCNKB
Accession:NM_000085
Location:INTRON

Gene Symbol:CLCNKB
Accession:NM_001165945
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001614800 CLINVAR
dbSNP (RS) rs869704 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCNKB CLINVAR
  LOC106501713 CLINVAR
OMIM 602023 CLINVAR