RGD:15120140 Rat Genome Database

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Variant: RGD:15120140 -  Homo sapiens

RGD ID: 15120140
RS ID: rs996273459
ClinVar ID: CV761000
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: USP9X  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 41,029,239
GRCh38 X 41,169,986
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001039590.3:c.2637-9T>C
NM_001039591.3:c.2637-9T>C
NG_012547.1:g.89352T>C
NC_000023.11:g.41169986T>C
More... 		08/01/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:USP9X
Accession:XM_005272675
Location:INTRON

Gene Symbol:USP9X
Accession:NM_001410748
Location:INTRON

Gene Symbol:USP9X
Accession:NM_001410749
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:USP9X
Accession:XM_005272676
Location:INTRON

Gene Symbol:USP9X
Accession:NM_001039590
Location:INTRON

Gene Symbol:USP9X
Accession:XM_047442548
Location:INTRON

Gene Symbol:USP9X
Accession:NM_001039591
Location:INTRON

Gene Symbol:USP9X
Accession:XM_047442550
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000918267 CLINVAR
dbSNP (RS) rs996273459 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene USP9X CLINVAR
OMIM 300072 CLINVAR