Variant #0000442808 (NC_000012.11:g.111353547G>T, NM_000432.3:c.141C>A (MYL2))

Chromosome 12
Allele Parent #1
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.111353547G>T
DNA change (hg38) g.110915743G>T
Published as -
ISCN -
DB-ID MYL2_000004 See all 3 reported entries
Variant remarks expression cloning
Reference PubMed: Szczesna-Cordary
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00017 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 2012-03-26 16:34:45 +02:00 (CEST)
Date last edited 2020-07-03 09:51:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 +/. 3 c.141C>A r.(?) p.Asn47Lys


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.