RGD:150404527 Rat Genome Database

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Variant: RGD:150404527 -  Homo sapiens

RGD ID: 150404527
RS ID: rs150119910
ClinVar ID: CV1194968
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PPIB  SNX22  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 15 64,448,524
GRCh38 15 64,156,325
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NR_073534.2:n.2491C>T
LRG_10:g.11831G>A
NC_000015.9:g.64448524C>T
NM_024798.3:c.*1817C>T
More... 		11/05/2018 3 prime utr variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SNX22
Accession:NM_024798
Location:3UTRS;EXON

Gene Symbol:SNX22
Accession:XM_017022581
Location:3UTRS;EXON

Gene Symbol:SNX22
Accession:NR_073534
Location:EXON;NON-CODING

Gene Symbol:PPIB
Accession:NM_000942
Location:INTRON

Gene Symbol:SNX22
Accession:XM_005254677
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001571202 CLINVAR
dbSNP (RS) rs150119910 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene PPIB CLINVAR
  SNX22 CLINVAR
OMIM 123841 CLINVAR