Variant #0000253357 (NC_000010.10:g.69882038A>G, NM_032578.3:c.843A>G (MYPN))

Chromosome 10
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.69882038A>G
DNA change (hg38) g.68122281A>G
Published as MYPN(NM_032578.3):c.843A>G (p.P281=), MYPN(NM_032578.4):c.843A>G (p.P281=)
ISCN -
DB-ID MYPN_000038 See all 4 reported entries
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) 0.00886 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYPN NM_032578.3 -/. - c.843A>G r.(?) p.(Pro281=)


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