Variant #0001050667 (NC_000002.11:g.61259135A>G, NM_002618.3:c.674A>G (PEX13))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61259135A>G
DNA change (hg38) -
Published as PEX13(NM_002618.4):c.674A>G (p.(Asp225Gly))
ISCN -
DB-ID PEX13_000028
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00159 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX13 NM_002618.3 -?/. - c.674A>G r.(?) p.(Asp225Gly)
PUS10 NM_144709.2 -?/. - c.-14008T>C r.(?) p.(=)


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