Variant #0000505919 (NC_000001.10:g.2337254C>T, NM_153818.1:c.992G>A (PEX10))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2337254C>T
DNA change (hg38) g.2405815C>T
Published as PEX10(NM_153818.1):c.992G>A (p.R331Q)
ISCN -
DB-ID PEX10_000021 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-09-08 13:49:09 +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.*2691C>T r.(=) p.(=)
PEX10 NM_153818.1 +?/. - c.992G>A r.(?) p.(Arg331Gln)


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