RGD:11597538 Rat Genome Database

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Variant: RGD:11597538 -  Homo sapiens

RGD ID: 11597538
ClinVar ID: CV292253
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WNT5A  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 55,500,375
GRCh38 3 55,466,347
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
NM_003392.4:c.*3745C>T
NG_031992.1:g.26296C>T
NC_000003.12:g.55466347G>A
NC_000003.11:g.55500375G>A
More... 		06/14/2016 3 prime utr variant likely benign infancy <1 / 1 000 000 WNT5A-Related Robinow Syndrome, Autosomal Dominant

Variant Details
Variant Transcripts
Gene Symbol:WNT5A
Accession:XM_017007127
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:NM_001256105
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448853
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448857
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448858
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_011534089
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448861
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_011534086
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_011534088
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:NM_001377271
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448852
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:NM_001377272
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:NM_003392
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448854
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448856
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_017007128
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448855
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448862
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448860
Location:3UTRS;EXON

Gene Symbol:WNT5A
Accession:XM_047448859
Location:3UTRS;EXON

Variant Samples