Variant #0000517643 (NC_000003.11:g.123457839del, NM_053025.3:c.493del (MYLK))

Chromosome 3
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.123457839del
DNA change (hg38) g.123738992del
Published as MYLK(NM_053025.3):c.493delA (p.(Thr165fs)), MYLK(NM_053025.3):c.493delA (p.T165Pfs*72), MYLK(NM_053025.4):c.493delA (p.T165Pfs*72)
ISCN -
DB-ID MYLK_000191 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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYLK NM_053025.3 ?/. - c.493del r.(?) p.(Thr165ProfsTer72)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.