RGD:11654919 Rat Genome Database

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Variant: RGD:11654919 -  Homo sapiens

RGD ID: 11654919
RS ID: rs369689471
ClinVar ID: CV343757
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CDH1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 16 68,868,687
GRCh38 16 68,834,784
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
LRG_301:g.102493T>C
NG_008021.1:g.102493T>C
NC_000016.10:g.68834784T>C
NC_000016.9:g.68868687T>C
More...
06/14/2016 3 prime utr variant uncertain significance adult 1-9 / 100 000 Hereditary diffuse gastric cancer
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:CDH1
Accession:NM_004360
Location:3UTRS;EXON

Gene Symbol:CDH1
Accession:NM_001317185
Location:3UTRS;EXON

Gene Symbol:CDH1
Accession:NM_001317186
Location:3UTRS;EXON

Gene Symbol:CDH1
Accession:NM_001317184
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000321792 CLINVAR
dbSNP (RS) rs369689471 CLINVAR
MedGen C1708349 CLINVAR
NCBI Gene CDH1 CLINVAR
OMIM 137215 CLINVAR
  192090 CLINVAR