RGD:14729229 Rat Genome Database

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Variant: RGD:14729229 -  Homo sapiens

RGD ID: 14729229
RS ID: rs113738936
ClinVar ID: CV664597
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RBM20  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 112,580,844
GRCh38 10 110,821,086
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001134363.3:c.2656-189C>T
NG_021177.1:g.181690C>T
NC_000010.11:g.110821086C>T
NC_000010.10:g.112580844C>T
More... 		06/19/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RBM20
Accession:XM_047425116
Location:INTRON

Gene Symbol:RBM20
Accession:NM_001134363
Location:INTRON

Gene Symbol:RBM20
Accession:XM_017016103
Location:INTRON

Gene Symbol:RBM20
Accession:XM_017016104
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000835127 CLINVAR
dbSNP (RS) rs113738936 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RBM20 CLINVAR
OMIM 613171 CLINVAR