Variant #0000998449 (NC_000010.10:g.69881639dup, NM_032578.3:c.444dup (MYPN))

Chromosome 10
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.69881639dup
DNA change (hg38) -
Published as MYPN(NM_001256267.1):c.444dupA (p.(Val149fs)), MYPN(NM_032578.4):c.444dupA (p.V149Sfs*5)
ISCN -
DB-ID MYPN_000188 See all 3 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYPN NM_032578.3 ?/. - c.444dup r.(?) p.(Val149SerfsTer5)


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