Variant #0000544211 (NC_000011.9:g.47359281dup, NM_000256.3:c.2373dup (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47359281dup
DNA change (hg38) g.47337730dup
Published as MYBPC3(NM_000256.3):c.2372delAinsAG (p.W792Vfs*41), MYBPC3(NM_000256.3):c.2373dupG (p.(Trp792Valfs*41)), MYBPC3(NM_000256.3):c.2373dupG (p.W792Vfs*41)
ISCN -
DB-ID MYBPC3_000149 See all 23 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 +/. - c.2373dup r.(?) p.(Trp792ValfsTer41)


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