RGD:13489107 Rat Genome Database

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Variant: RGD:13489107 -  Homo sapiens

RGD ID: 13489107
RS ID: rs1554060095
ClinVar ID: CV454080
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 5 112,043,036
GRCh38 5 112,707,339
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NM_000038.5:c.-30605A>T
NC_000005.10:g.112707339A>T
NC_000005.9:g.112043036A>T
LRG_130:g.19819A>T
More... 		08/08/2017 uncertain significance APC-Associated Polyposis Conditions; FAMILIAL ADENOMATOUS POLYPOSIS 1, ATTENUATED; POLYPOSIS, ADENOMATOUS INTESTINAL
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003651967 CLINVAR
dbSNP (RS) rs1554060095 CLINVAR
MedGen C2713442 CLINVAR
NCBI Gene APC CLINVAR
OMIM 175100 CLINVAR
  611731 CLINVAR