Variant #0000723451 (NC_000011.9:g.45936235T>C, PEX16(NM_057174.2):c.461A>G)

Chromosome 11
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.45936235T>C
DNA change (hg38) -
Published as PEX16(NM_057174.2):c.461A>G (p.D154G)
ISCN -
DB-ID PEX16_000023
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) 6.0E-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     
PEX16 NM_004813.2 ?/. - c.461A>G r.(?) p.(Asp154Gly)
PEX16 NM_057174.2 ?/. - c.461A>G r.(?) p.(Asp154Gly)