RGD:14736693 Rat Genome Database

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Variant: RGD:14736693 -  Homo sapiens

RGD ID: 14736693
RS ID: rs77994621
ClinVar ID: CV662745
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCN1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 143,043,818
GRCh38 7 143,346,725
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000083.3:c.2364+67G>A
NG_009815.1:g.35600G>A
NC_000007.14:g.143346725G>A
NC_000007.13:g.143043818G>A
More... 		06/19/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CLCN1
Accession:NM_000083
Location:INTRON

Gene Symbol:CLCN1
Accession:NR_046453
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838591 CLINVAR
dbSNP (RS) rs77994621 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CLCN1 CLINVAR
OMIM 118425 CLINVAR