RGD:11655408 Rat Genome Database

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Variant: RGD:11655408 -  Homo sapiens

RGD ID: 11655408
RS ID: rs886047735
ClinVar ID: CV325307
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 118,175,385
GRCh38 11 118,304,670
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_38t1:c.-166G>A
LRG_38:g.5091G>A
NG_007383.1:g.5091G>A
NC_000011.10:g.118304670G>A
More... 		01/12/2018 5 prime utr variant uncertain significance CD3-EPSILON DEFICIENCY; CD3epsilon deficiency
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000325470 CLINVAR
dbSNP (RS) rs886047735 CLINVAR
MedGen C3810127 CLINVAR
NCBI Gene CD3E CLINVAR
OMIM 186830 CLINVAR
  615615 CLINVAR