RGD:11646239 Rat Genome Database

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Variant: RGD:11646239 -  Homo sapiens

RGD ID: 11646239
RS ID: rs886046720
ClinVar ID: CV320241
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RBM20  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 10 112,598,264
GRCh38 10 110,838,506
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_382:g.199110C>A
NG_021177.1:g.199110C>A
NC_000010.11:g.110838506C>A
NC_000010.10:g.112598264C>A
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:RBM20
Accession:XM_017016104
Location:3UTRS;EXON

Gene Symbol:RBM20
Accession:XM_017016103
Location:3UTRS;EXON

Gene Symbol:RBM20
Accession:NM_001134363
Location:3UTRS;EXON

Gene Symbol:RBM20
Accession:XM_047425116
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000269559 CLINVAR
dbSNP (RS) rs886046720 CLINVAR
MedGen C2750995 CLINVAR
NCBI Gene RBM20 CLINVAR
OMIM 613171 CLINVAR
  613172 CLINVAR