RGD:28890738 Rat Genome Database

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Variant: RGD:28890738 -  Homo sapiens

RGD ID: 28890738
RS ID: rs1641399279
ClinVar ID: CV865125
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HSPG2  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 22,206,852
GRCh38 1 21,880,359
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_005529.7:c.2195+4C>A
NC_000001.10:g.22206852G>T
NM_005529.5:c.2195+4C>A
NM_001291860.2:c.2198+4C>A
More... 		01/13/2018 intron variant uncertain significance Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type; Dyssegmental dwarfism Silverman-Handmaker type; Dyssegmental Dysplasia; Myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HSPG2
Accession:NM_005529
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_017001120
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_047419090
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_017001122
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_047419080
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_047419091
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_011541318
Location:INTRON

Gene Symbol:HSPG2
Accession:XM_017001121
Location:INTRON

Gene Symbol:HSPG2
Accession:NM_001291860
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001099914 CLINVAR
  RCV001099915 CLINVAR
dbSNP (RS) rs1641399279 CLINVAR
MedGen C0036391 CLINVAR
  C1857100 CLINVAR
NCBI Gene HSPG2 CLINVAR
OMIM 142461 CLINVAR
  224410 CLINVAR
  255800 CLINVAR
SNOMED CT 93132001 CLINVAR