RGD:14735829 Rat Genome Database

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Variant: RGD:14735829 -  Homo sapiens

RGD ID: 14735829
RS ID: rs4918595
ClinVar ID: CV664594
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RBM20  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 10 112,583,606
GRCh38 10 110,823,848
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.3451+234A>G
NG_021177.1:g.184452A>G
NC_000010.11:g.110823848A>G
NC_000010.10:g.112583606A>G
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RBM20
Accession:NM_001134363
Location:INTRON

Gene Symbol:RBM20
Accession:XM_017016103
Location:INTRON

Gene Symbol:RBM20
Accession:XM_047425116
Location:INTRON

Gene Symbol:RBM20
Accession:XM_017016104
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838195 CLINVAR
dbSNP (RS) rs4918595 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RBM20 CLINVAR
OMIM 613171 CLINVAR