RGD:11629824 Rat Genome Database

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Variant: RGD:11629824 -  Homo sapiens

RGD ID: 11629824
RS ID: rs141229564
ClinVar ID: CV351118
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PEX26  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 18,571,305
GRCh38 22 18,088,539
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
NG_008339.1:g.15620A>G
NC_000022.11:g.18088539A>G
NC_000022.10:g.18571305A>G
NM_017929.6:c.*464A>G
More... 		01/13/2018 3 prime utr variant benign|likely benign neonatal Peroxisome biogenesis disorder 7A
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:PEX26
Accession:NM_017929
Location:3UTRS;EXON

Gene Symbol:PEX26
Accession:NM_001199319
Location:3UTRS;EXON

Gene Symbol:PEX26
Accession:NM_001127649
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000334452 CLINVAR
dbSNP (RS) rs141229564 CLINVAR
MedGen C3888385 CLINVAR
NCBI Gene PEX26 CLINVAR
OMIM 608666 CLINVAR
  614872 CLINVAR