RGD:14708820 Rat Genome Database

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Variant: RGD:14708820 -  Homo sapiens

RGD ID: 14708820
RS ID: rs951801692
ClinVar ID: CV656049
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CTSD  LOC130005119  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 1,785,095
GRCh38 11 1,763,865
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001909.5:c.-6G>T
NG_008655.1:g.5128G>T
NC_000011.10:g.1763865C>A
NC_000011.9:g.1785095C>A
More... 		05/04/2018 5 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CTSD
Accession:NM_001909
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000827263 CLINVAR
dbSNP (RS) rs951801692 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene CTSD CLINVAR
  LOC130005119 CLINVAR
OMIM 116840 CLINVAR