RGD:405164100 Rat Genome Database

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Variant: RGD:405164100 -  Homo sapiens

RGD ID: 405164100
ClinVar ID: CV3160401
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: APC  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 5 112,173,916
GRCh38 5 112,838,219
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001407471.1:c.1473G>A
NM_001407472.1:c.1473G>A
NM_001354906.2:c.1776G>A
NM_001407470.1:c.1776G>A
More... 		01/16/2024 non-coding transcript variant likely benign 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 RCV003857280 CLINVAR
MedGen C2713442 CLINVAR
NCBI Gene APC CLINVAR
OMIM 175100 CLINVAR
  611731 CLINVAR