Variant #0000350432 (NC_000003.11:g.123453061A>G, NM_053025.3:c.782T>C (MYLK))

Chromosome 3
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.123453061A>G
DNA change (hg38) g.123734214A>G
Published as MYLK(NM_053025.3):c.782T>C (p.V261A), MYLK(NM_053025.4):c.782T>C (p.V261A)
ISCN -
DB-ID MYLK_000114 See all 3 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) 0.11364 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
MYLK NM_053025.3 -/. - c.782T>C r.(?) p.(Val261Ala)


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