Variant #0000299754 (NC_000012.11:g.111357011G>A, NC_000012.11(NM_000432.3):c.4-14C>T (MYL2))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.111357011G>A
DNA change (hg38) g.110919207G>A
Published as MYL2(NM_000432.3):c.4-14C>T, MYL2(NM_000432.4):c.4-14C>T
ISCN -
DB-ID MYL2_000054 See all 4 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) 0.00962 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYL2 NM_000432.3 -/. - c.4-14C>T r.(=) p.(=)


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