Variant #0000562401 (NC_000017.10:g.56350849T>C, NM_000250.1:c.1547A>G (MPO))

Chromosome 17
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.56350849T>C
DNA change (hg38) g.58273488T>C
Published as MPO(NM_000250.1):c.1547A>G (p.Y516C)
ISCN -
DB-ID MPO_000017
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPO NM_000250.1 ?/. - c.1547A>G r.(?) p.(Tyr516Cys)
LPO NM_001160102.1 ?/. - c.*5494T>C r.(=) p.(=)


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