Variant #0000452323 (NC_000010.10:g.69881254A>G, NM_032578.3:c.59A>G (MYPN))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.69881254A>G
DNA change (hg38) g.68121497A>G
Published as -
ISCN -
DB-ID MYPN_000023 See all 10 reported entries
Variant remarks expression cloning neonatal rat cardiomyocytes, normal Z-disc assembly, impaired nuclear localisation
Reference PubMed: Purevjav 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00095 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 2012-04-27 16:57:10 +02:00 (CEST)
Date last edited 2020-07-14 21:56:45 +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 +?/. 2 c.59A>G r.(?) p.Tyr20Cys


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