Variant #0000452326 (NC_000010.10:g.69959174C>T, NM_032578.3:c.3335C>T (MYPN))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.69959174C>T
DNA change (hg38) g.68199417C>T
Published as -
ISCN -
DB-ID MYPN_000003 See all 11 reported entries
Variant remarks eGFP expression cloning RNC cells sarcomeric apparatus disorganization, abnormal cells, reduced cell survival
Reference PubMed: Duboscq-Bidot 2008
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00319 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2012-04-06 19:06:29 +02:00 (CEST)
Date last edited 2020-07-14 21:57:48 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYPN NM_032578.3 +/. 17 c.3335C>T r.(?) p.Pro1112Leu


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