RGD:150441330 Rat Genome Database

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Variant: RGD:150441330 -  Homo sapiens

RGD ID: 150441330
RS ID: rs59006537
ClinVar ID: CV1265764
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCNKB  LOC106501713  
Reference Nucleotide: -
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 16,376,230
GRCh38 1 16,049,735
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.359+33_359+34insT
NC_000001.11:g.16049735_16049736insT
NC_000001.10:g.16376230_16376231insT
NM_000085.5:c.866+33_866+34insT
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 RCV001690489 CLINVAR
dbSNP (RS) rs59006537 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCNKB CLINVAR
  LOC106501713 CLINVAR
OMIM 602023 CLINVAR