Variant #0000296907 (NC_000011.9:g.45936035G>A, PEX16(NM_057174.2):c.542-16C>T)

Chromosome 11
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.45936035G>A
DNA change (hg38) g.45914484G>A
Published as PEX16(NM_004813.4):c.542-16C>T
ISCN -
DB-ID PEX16_000013 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) 0.8032 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     
PEX16 NM_004813.2 -/. - c.542-16C>T r.(=) p.(=)
PEX16 NM_057174.2 -/. - c.542-16C>T r.(=) p.(=)