RGD:11630662 Rat Genome Database

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Variant: RGD:11630662 -  Homo sapiens

RGD ID: 11630662
RS ID: rs9623286
ClinVar ID: CV352591
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: XPNPEP3  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 41,326,801
GRCh38 22 40,930,797
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028221.1:g.78717C>G
NC_000022.11:g.40930797C>G
NC_000022.10:g.41326801C>G
NM_022098.4:c.*4362C>G
More... 		01/13/2018 3 prime utr variant benign|likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:XPNPEP3
Accession:NM_022098
Location:3UTRS;EXON

Gene Symbol:XPNPEP3
Accession:NM_001204827
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000355257 CLINVAR
dbSNP (RS) rs9623286 CLINVAR
MedGen C3150419 CLINVAR
NCBI Gene XPNPEP3 CLINVAR
OMIM 613159 CLINVAR
  613553 CLINVAR