Variant #0000690372 (NC_000009.11:g.113563143G>T, NM_005592.3:c.2485G>T (MUSK))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.113563143G>T
DNA change (hg38) -
Published as MUSK(NM_001166280.1):c.2227G>T (p.(Val743Leu))
ISCN -
DB-ID MUSK_000047
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) 0.04339 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2020-09-15 15:50:26 +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     
MUSK NM_005592.3 -?/. - c.2485G>T r.(?) p.(Val829Leu)


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