Variant #0001049869 (NC_000001.10:g.2338177C>T, NM_153818.1:c.818G>A (PEX10))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.2338177C>T
DNA change (hg38) -
Published as PEX10(NM_002617.4):c.758G>A (p.(Arg253His))
ISCN -
DB-ID PEX10_000084
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) 6.0E-5 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     
RER1 NM_007033.4 ?/. - c.*3614C>T r.(=) p.(=)
PEX10 NM_153818.1 ?/. - c.818G>A r.(?) p.(Arg273His)


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