RGD:11658377 Rat Genome Database

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Variant: RGD:11658377 -  Homo sapiens

RGD ID: 11658377
RS ID: rs886045806
ClinVar ID: CV279613
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 201,081,673
GRCh38 1 201,112,545
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000001.11:g.201112545G>A
NC_000001.10:g.201081673G>A
NG_009816.2:g.5022C>T
NM_000069.2:c.-206C>T
 06/14/2016 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000348672 CLINVAR
dbSNP (RS) rs886045806 CLINVAR
MedGen C0238358 CLINVAR
NCBI Gene CACNA1S CLINVAR
OMIM 114208 CLINVAR
  170400 CLINVAR