Variant #0000690844 (NC_000010.10:g.95079645_95079646dup, NM_013451.3:c.5582_5583dup (MYOF))

Chromosome 10
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.95079645_95079646dup
DNA change (hg38) -
Published as MYOF(NM_013451.4):c.5582_5583dupGT (p.I1862Vfs*23)
ISCN -
DB-ID MYOF_000014
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYOF NM_013451.3 ?/. - c.5582_5583dup r.(?) p.(Ile1862ValfsTer23)


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