RGD:150462611 Rat Genome Database

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Variant: RGD:150462611 -  Homo sapiens

RGD ID: 150462611
RS ID: rs150294043
ClinVar ID: CV1206614
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RBM10  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 X 47,044,394
GRCh38 X 47,184,995
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_152856.3:c.1717-60G>C
NM_001204466.2:c.1720-60G>C
NM_001204467.2:c.1948-60G>C
NM_005676.5:c.1951-60G>C
More... 		07/15/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RBM10
Accession:NM_001204468
Location:INTRON

Gene Symbol:RBM10
Accession:XM_005272677
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442554
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442552
Location:INTRON

Gene Symbol:RBM10
Accession:NM_152856
Location:INTRON

Gene Symbol:RBM10
Accession:NM_001204467
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442551
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442555
Location:INTRON

Gene Symbol:RBM10
Accession:XM_005272678
Location:INTRON

Gene Symbol:RBM10
Accession:XM_005272679
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442553
Location:INTRON

Gene Symbol:RBM10
Accession:NM_001204466
Location:INTRON

Gene Symbol:RBM10
Accession:NM_005676
Location:INTRON

Gene Symbol:RBM10
Accession:XM_047442556
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001587015 CLINVAR
dbSNP (RS) rs150294043 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RBM10 CLINVAR
OMIM 300080 CLINVAR