RGD:150487606 Rat Genome Database

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Variant: RGD:150487606 -  Homo sapiens

RGD ID: 150487606
RS ID: rs9642837
ClinVar ID: CV1251551
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXT1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 118,842,744
GRCh38 8 117,830,505
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000127.3:c.1165-156G>T
LRG_493:g.286315G>T
NG_007455.2:g.286315G>T
NC_000008.11:g.117830505C>A
More... 		08/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EXT1
Accession:NM_000127
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001674222 CLINVAR
dbSNP (RS) rs9642837 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EXT1 CLINVAR
OMIM 608177 CLINVAR