Variant #0000292780 (NC_000012.11:g.111350901T>G, NM_000432.3:c.401A>C (MYL2))

Chromosome 12
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.111350901T>G
DNA change (hg38) g.110913097T>G
Published as MYL2(NM_000432.3):c.401A>C (p.E134A), MYL2(NM_000432.4):c.401A>C (p.E134A)
ISCN -
DB-ID MYL2_000014 See all 14 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) 0.00019 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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 ?/. - c.401A>C r.(?) p.(Glu134Ala)


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