RGD:11578316 Rat Genome Database

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Variant: RGD:11578316 -  Homo sapiens

RGD ID: 11578316
RS ID: rs202242499
ClinVar ID: CV268588
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CHST3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 73,768,236
GRCh38 10 72,008,478
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Prevalence Trait Synonyms
NG_012635.1:g.49117C>T
NC_000010.11:g.72008478C>T
NC_000010.10:g.73768236C>T
NM_004273.4:c.*7C>T
More... 		06/14/2016 3 prime utr variant benign|likely benign infancy <1 / 1 000 000 AllHighlyPenetrant; Bilateral dislocation of the knees, pes cavus, cylindrically shaped fingers and characteristic facies; Humero-spinal dysostosis with congenital heart disease; Kozlowski Celermajer Tink syndrome; Larsen syndrome, dominant type; Primary bone dysplasia; SED congenita; Spondyloepiphyseal dysplasia, congenital type
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype

Variant Details
Variant Transcripts
Gene Symbol:CHST3
Accession:NM_004273
Location:3UTRS;EXON

Gene Symbol:CHST3
Accession:XM_047426022
Location:3UTRS;EXON

Gene Symbol:CHST3
Accession:XM_011540369
Location:3UTRS;EXON

Gene Symbol:CHST3
Accession:XM_006718075
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000278793 CLINVAR
  RCV000282169 CLINVAR
  RCV000337241 CLINVAR
  RCV000373254 CLINVAR
  RCV000393419 CLINVAR
dbSNP (RS) rs202242499 CLINVAR
MedGen C0175778 CLINVAR
  C0410528 CLINVAR
  C1837657 CLINVAR
  C2745959 CLINVAR
  CN169374 CLINVAR
NCBI Gene CHST3 CLINVAR
OMIM 143095 CLINVAR
  150250 CLINVAR
  183900 CLINVAR
  603799 CLINVAR
SNOMED CT 105986008 CLINVAR
  63387002 CLINVAR