RGD:11634554 Rat Genome Database

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Variant: RGD:11634554 -  Homo sapiens

RGD ID: 11634554
ClinVar ID: CV286641
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 47,596,296
GRCh38 2 47,369,157
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_215t1:c.-349G>T
NM_002354.2:c.-349G>T
LRG_215:g.28995G>T
NG_012352.2:g.28995G>T
More...
06/14/2016 5 prime utr variant uncertain significance Colorectal cancer, hereditary nonpolyposis; Familial nonpolyposis colon cancer

Variant Details
Variant Samples