RGD:150417883 Rat Genome Database

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Variant: RGD:150417883 -  Homo sapiens

RGD ID: 150417883
RS ID: rs112114912
ClinVar ID: CV1192728
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCNKB  LOC106501713  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 16,382,546
GRCh38 1 16,056,051
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001165945.2:c.1419+293C>T
NM_000085.5:c.1929+293C>T
NG_042865.1:g.11559C>T
NG_013079.1:g.17300C>T
More... 		11/10/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CLCNKB
Accession:NM_001165945
Location:INTRON

Gene Symbol:CLCNKB
Accession:NM_000085
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001568965 CLINVAR
dbSNP (RS) rs112114912 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCNKB CLINVAR
  LOC106501713 CLINVAR
OMIM 602023 CLINVAR