Variant #0000296902 (NC_000001.10:g.2337277C>T, PEX10(NM_153818.1):c.973-4G>A)

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2337277C>T
DNA change (hg38) g.2405838C>T
Published as PEX10(NM_153818.1):c.973-4G>A
ISCN -
DB-ID PEX10_000041
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.10492 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RER1 NM_007033.4 -/. - c.*2714C>T r.(=) p.(=)
PEX10 NM_153818.1 -/. - c.973-4G>A r.spl? p.?