RGD:150456466 Rat Genome Database

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Variant: RGD:150456466 -  Homo sapiens

RGD ID: 150456466
RS ID: rs2863437
ClinVar ID: CV1219491
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCNKB  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 1 16,370,664
GRCh38 1 16,044,169
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.-8+289T>G
NG_013079.1:g.5418T>G
NC_000001.11:g.16044169T>G
NC_000001.10:g.16370664T>G
 11/10/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CLCNKB
Accession:NM_000085
Location:5UTRS;INTRON

Gene Symbol:CLCNKB
Accession:NM_001165945
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001612706 CLINVAR
dbSNP (RS) rs2863437 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCNKB CLINVAR
OMIM 602023 CLINVAR