RGD:153347853 Rat Genome Database

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Variant: RGD:153347853 -  Homo sapiens

RGD ID: 153347853
RS ID: rs1034087679
ClinVar ID: CV1694901
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WDR35  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 20,160,310
GRCh38 2 19,960,549
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_021212.1:g.34575G>A
NM_001006657.1:c.1288+5G>A
NC_000002.11:g.20160310C>T
NC_000002.12:g.19960549C>T
More... 		12/01/2019 intron variant uncertain significance Connective tissue disease
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:WDR35
Accession:XM_011533007
Location:5UTRS;INTRON

Gene Symbol:WDR35
Accession:XM_047445199
Location:INTRON

Gene Symbol:WDR35
Accession:NM_020779
Location:INTRON

Gene Symbol:WDR35
Accession:NM_001006657
Location:INTRON

Gene Symbol:WDR35
Accession:XR_426989
Location:INTRON;NON-CODING

Gene Symbol:WDR35
Accession:XR_939699
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002278832 CLINVAR
dbSNP (RS) rs1034087679 CLINVAR
MedGen C0009782 CLINVAR
NCBI Gene WDR35 CLINVAR
OMIM 613602 CLINVAR