RGD:11654912 Rat Genome Database

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Variant: RGD:11654912 -  Homo sapiens

RGD ID: 11654912
RS ID: rs886057244
ClinVar ID: CV352135
Genic Status: INTERGENIC
Type: SNV (SO:0001483) 
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 22 18,560,728
GRCh38 22 18,077,962
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Age of Onset Trait Synonyms
NC_000022.11:g.18077962C>T
NC_000022.10:g.18560728C>T
NM_001199319.1:c.-167C>T
NM_017929.5:c.-167C>T
More... 		01/13/2018 2kb upstream variant|5 prime utr variant uncertain significance neonatal Peroxisome biogenesis disorder 7A
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000321765 CLINVAR
dbSNP (RS) rs886057244 CLINVAR
MedGen C3888385 CLINVAR
NCBI Gene PEX26 CLINVAR
OMIM 608666 CLINVAR
  614872 CLINVAR