Variant #0000723450 (NC_000011.9:g.45931671G>A, PEX16(NM_057174.2):c.1010C>T)

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.45931671G>A
DNA change (hg38) -
Published as PEX16(NM_057174.2):c.1010C>T (p.S337L)
ISCN -
DB-ID C11orf94_000008
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) 5.0E-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     
C11orf94 NM_001080446.2 -?/. - c.-2875C>T r.(?) p.(=)
PEX16 NM_004813.2 -?/. - c.*134C>T r.(=) p.(=)
MAPK8IP1 NM_005456.3 -?/. - c.*4399G>A r.(=) p.(=)
PEX16 NM_057174.2 -?/. - c.1010C>T r.(?) p.(Ser337Leu)