Variant #0001049321 (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) -
Published as -
ISCN -
DB-ID MYL2_000014 See all 14 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs143139258
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00019 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-13 14:55:01 +02:00 (CEST)
Date last edited N/A
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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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