RGD:150464446 Rat Genome Database

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Variant: RGD:150464446 -  Homo sapiens

RGD ID: 150464446
RS ID: rs576064910
ClinVar ID: CV1214949
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCNKB  LOC106501713  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 16,378,100
GRCh38 1 16,051,605
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.1297+58C>A
NM_001165945.2:c.790+58C>A
NG_013079.1:g.12854C>A
NG_042865.1:g.7113C>A
More... 		11/10/2018 intron variant 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 RCV001613946 CLINVAR
dbSNP (RS) rs576064910 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCNKB CLINVAR
  LOC106501713 CLINVAR
OMIM 602023 CLINVAR