RGD:407515509 Rat Genome Database

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Variant: RGD:407515509 -  Homo sapiens

RGD ID: 407515509
ClinVar ID: CV3440952
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IL10RA  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 117,870,238
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_151t1:c.1619G>T
NM_001558.4:c.1619G>T
LRG_151:g.18133G>T
NG_016275.1:g.18133G>T
More... 		05/21/2024 missense variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004627916 CLINVAR
MedGen C0950123 CLINVAR
NCBI Gene IL10RA CLINVAR
OMIM 146933 CLINVAR