RGD:13509151 Rat Genome Database

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Variant: RGD:13509151 -  Homo sapiens

RGD ID: 13509151
RS ID: rs747009288
ClinVar ID: CV481828
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: OTUD6B  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 92,096,343
GRCh38 8 91,084,115
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000008.11:g.91084115G>A
NC_000008.10:g.92096343G>A
NM_001286745.3:c.494+1G>A
NM_001416022.1:c.716+1G>A
More... 		01/22/2018 splice donor variant pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:OTUD6B
Accession:NM_016023
Location:INTRON

Gene Symbol:OTUD6B
Accession:NM_001286745
Location:INTRON

Gene Symbol:OTUD6B
Accession:XM_011517129
Location:INTRON

Gene Symbol:OTUD6B
Accession:XM_047421864
Location:INTRON

Gene Symbol:OTUD6B
Accession:NM_001416022
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000579017 CLINVAR
dbSNP (RS) rs747009288 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene OTUD6B CLINVAR
OMIM 612021 CLINVAR