RGD:11659217 Rat Genome Database

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Variant: RGD:11659217 -  Homo sapiens

RGD ID: 11659217
RS ID: rs886051696
ClinVar ID: CV340611
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CLCN7  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 16 1,496,277
GRCh38 16 1,446,276
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007567.1:g.33809C>T
NC_000016.10:g.1446276G>A
NC_000016.9:g.1496277G>A
NM_001287.6:c.*355C>T
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View
osteopetrosis  (IAGP)

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Osteopetrosis  (IAGP)

Variant Details
Variant Transcripts
Gene Symbol:CLCN7
Accession:NM_001287
Location:3UTRS;EXON

Gene Symbol:CLCN7
Accession:XM_011522354
Location:3UTRS;EXON

Gene Symbol:CLCN7
Accession:NM_001114331
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355774 CLINVAR
dbSNP (RS) rs886051696 CLINVAR
MedGen C0029454 CLINVAR
NCBI Gene CLCN7 CLINVAR
OMIM 602727 CLINVAR