RGD:28874209 Rat Genome Database

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Variant: RGD:28874209 -  Homo sapiens

RGD ID: 28874209
RS ID: rs924527994
ClinVar ID: CV891347
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: XPNPEP3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 41,326,195
GRCh38 22 40,930,191
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.78111A>G
NC_000022.11:g.40930191A>G
NC_000022.10:g.41326195A>G
NM_022098.4:c.*3756A>G
More...
01/13/2018 3 prime utr variant uncertain significance
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 RCV001147104 CLINVAR
dbSNP (RS) rs924527994 CLINVAR
MedGen C3150419 CLINVAR
NCBI Gene XPNPEP3 CLINVAR
OMIM 613159 CLINVAR
  613553 CLINVAR