RGD:11587403 Rat Genome Database

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Variant: RGD:11587403 -  Homo sapiens

RGD ID: 11587403
RS ID: rs536755317
ClinVar ID: CV278471
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 201,081,680
GRCh38 1 201,112,552
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.201112552C>T
NC_000001.10:g.201081680C>T
NG_009816.2:g.5015G>A
NM_000069.2:c.-213G>A
 06/14/2016 5 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000295041 CLINVAR
dbSNP (RS) rs536755317 CLINVAR
MedGen C0238358 CLINVAR
NCBI Gene CACNA1S CLINVAR
OMIM 114208 CLINVAR
  170400 CLINVAR