Variant #0000292352 (NC_000011.9:g.47353661del, NM_000256.3:c.3776del (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.47353661del
DNA change (hg38) g.47332110del
Published as MYBPC3(NM_000256.3):c.3776del (p.(Gln1259ArgfsTer72)), MYBPC3(NM_000256.3):c.3776delA (p.Q1259Rfs*72)
ISCN -
DB-ID MYBPC3_000188 See all 9 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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.3776del r.(?) p.(Gln1259ArgfsTer72)
MADD NM_003682.3 +/. - c.*2960del r.(?) p.(=)


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