Variant #0000286641 (NC_000017.10:g.56348106T>C, NM_000250.1:c.2149A>G (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.56348106T>C
DNA change (hg38) g.58270745T>C
Published as MPO(NM_000250.1):c.2149A>G (p.I717V)
ISCN -
DB-ID MPO_000002
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) 0.02388 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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MPO NM_000250.1 -/. - c.2149A>G r.(?) p.(Ile717Val)
LPO NM_001160102.1 -/. - c.*2751T>C r.(=) p.(=)


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