RGD:150463079 Rat Genome Database

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Variant: RGD:150463079 -  Homo sapiens

RGD ID: 150463079
RS ID: rs10495700
ClinVar ID: CV1235004
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: WDR35  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 20,166,965
GRCh38 2 19,967,204
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000002.12:g.19967204A>G
NC_000002.11:g.20166965A>G
NM_001006657.2:c.1009-295T>C
NM_020779.4:c.1009-295T>C
More... 		08/09/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:WDR35
Accession:NM_020779
Location:INTRON

Gene Symbol:WDR35
Accession:XM_047445199
Location:INTRON

Gene Symbol:WDR35
Accession:NM_001006657
Location:INTRON

Gene Symbol:WDR35
Accession:XM_011533007
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 Information

Database Acc Id Source(s)
ClinVar RCV001649586 CLINVAR
dbSNP (RS) rs10495700 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene WDR35 CLINVAR
OMIM 613602 CLINVAR