Variant #0000442801 (NC_000012.11:g.111356964C>T, NM_000432.3:c.37G>A (MYL2))

Chromosome 12
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.111356964C>T
DNA change (hg38) g.110919160C>T
Published as -
ISCN -
DB-ID MYL2_000001 See all 10 reported entries
Variant remarks in vitro expression cloning, 3x reduced Ca2+ binding properties, phosphorylation increases Ca2+ binding
Reference PubMed: Szczesna 2001
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00037 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 2010-07-23 17:13:31 +02:00 (CEST)
Date last edited 2020-07-03 09:51:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 +?/. 2 c.37G>A r.(?) p.Ala13Thr


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