RGD:151740856 Rat Genome Database

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Variant: RGD:151740856 -  Homo sapiens

RGD ID: 151740856
RS ID: rs1811889441
ClinVar ID: CV1478021
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXT1  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 8 118,831,914
GRCh38 8 117,819,675
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.1536+1G>C
LRG_493:g.297145G>C
NG_007455.2:g.297145G>C
NC_000008.11:g.117819675C>G
More... 		07/13/2021 splice donor variant pathogenic Hereditary multiple exostoses; Hereditary multiple exostosis; Hereditary multiple osteochondromas; MULTIPLE CARTILAGINOUS EXOSTOSES; Multiple exostoses; Multiple osteochondromas
Disease Annotations     Click to see Annotation Detail View

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

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

Variant Samples
Additional References at PubMed
PMID:10679937   PMID:11391482   PMID:16199547   PMID:16283885   PMID:19810120   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001947090 CLINVAR
dbSNP (RS) rs1811889441 CLINVAR
MedGen C0015306 CLINVAR
NCBI Gene EXT1 CLINVAR
OMIM 133700 CLINVAR
  608177 CLINVAR
SNOMED CT 254044004 CLINVAR