Variant #0000280329 (NC_000011.9:g.47353740G>A, NM_000256.3:c.3697C>T (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.47353740G>A
DNA change (hg38) g.47332189G>A
Published as MYBPC3(NM_000256.3):c.3697C>T (p.Q1233*)
ISCN -
DB-ID MYBPC3_000287 See all 12 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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.3697C>T r.(?) p.(Gln1233Ter)
MADD NM_003682.3 +/. - c.*3039G>A r.(=) p.(=)


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