Variant #0000613342 (NC_000011.9:g.45939320C>T, PEX16(NM_057174.2):c.43G>A)

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.45939320C>T
DNA change (hg38) g.45917769C>T
Published as PEX16(NM_004813.3):c.43G>A (p.V15M)
ISCN -
DB-ID GYLTL1B_000024
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) Variant not found in online data sets
Owner VKGL-NL_AMC
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PEX16 NM_004813.2 ?/. - c.43G>A r.(?) p.(Val15Met)
PEX16 NM_057174.2 ?/. - c.43G>A r.(?) p.(Val15Met)
GYLTL1B NM_152312.3 ?/. - c.-3987C>T r.(?) p.(=)