rs571058325 Rat Genome Database

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Variant: rs571058325 -  Homo sapiens

RGD ID: 11599883
RS ID: rs571058325
ClinVar ID: CV313549
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ROR2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 94,485,386
GRCh38 9 91,723,104
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_008089.1:g.232059C>T
NC_000009.12:g.91723104G>A
NC_000009.11:g.94485386G>A
NM_004560.4:c.*558C>T
More... 		01/13/2018 3 prime utr variant likely benign|uncertain significance infancy <1 / 1 000 000 COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA; COVESDEM SYNDROME; ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 1
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ROR2
Accession:NM_004560
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_005252008
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_005252009
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_006717121
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_017014762
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_047423436
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_047423435
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_047423437
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:XM_047423434
Location:3UTRS;EXON

Gene Symbol:ROR2
Accession:NM_001318204
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000269046 CLINVAR
  RCV000324079 CLINVAR
dbSNP (RS) rs571058325 CLINVAR
MedGen C1862112 CLINVAR
  C5399974 CLINVAR
NCBI Gene ROR2 CLINVAR
OMIM 113000 CLINVAR
  268310 CLINVAR
  602337 CLINVAR