Variant #0000286640 (NC_000017.10:g.56348122G>A, NM_000250.1:c.2133C>T (MPO))

Chromosome 17
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.56348122G>A
DNA change (hg38) g.58270761G>A
Published as MPO(NM_000250.1):c.2133C>T (p.T711=)
ISCN -
DB-ID MPO_000003
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) 0.00415 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-14 08:47:22 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPO NM_000250.1 -/. - c.2133C>T r.(?) p.(Thr711=)
LPO NM_001160102.1 -/. - c.*2767G>A r.(=) p.(=)


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