Variant #0000717268 (NC_000001.10:g.2337219G>A, PEX10(NM_153818.1):c.1027C>T)

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.2337219G>A
DNA change (hg38) -
Published as PEX10(NM_153818.1):c.1027C>T (p.R343W)
ISCN -
DB-ID PEX10_000072
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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RER1 NM_007033.4 ?/. - c.*2656G>A r.(=) p.(=)
PEX10 NM_153818.1 ?/. - c.1027C>T r.(?) p.(Arg343Trp)