RGD:13483000 Rat Genome Database

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Variant: RGD:13483000 -  Homo sapiens

RGD ID: 13483000
RS ID: rs971869116
ClinVar ID: CV445162
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZIC2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 13 100,634,300
GRCh38 13 99,982,046
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_007085.3:g.5291G>C
NC_000013.11:g.99982046G>C
NC_000013.10:g.100634300G>C
NM_007129.5:c.-19G>C
More... 		08/04/2017 5 prime utr variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:ZIC2
Accession:NM_007129
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000521943 CLINVAR
dbSNP (RS) rs971869116 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ZIC2 CLINVAR
OMIM 603073 CLINVAR