Variant #0000505920 (NC_000001.10:g.2337996C>T, NM_153818.1:c.899G>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.2337996C>T
DNA change (hg38) g.2406557C>T
Published as PEX10(NM_002617.4):c.839G>A (p.(Arg280His)), PEX10(NM_153818.1):c.899G>A (p.R300H)
ISCN -
DB-ID PEX10_000062 See all 2 reported entries
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) 0.0001 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RER1 NM_007033.4 ?/. - c.*3433C>T r.(=) p.(=)
PEX10 NM_153818.1 ?/. - c.899G>A r.(?) p.(Arg300His)


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