Variant #0000544116 (NC_000011.9:g.47355233C>G, NM_000256.3:c.3065G>C (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47355233C>G
DNA change (hg38) g.47333682C>G
Published as MYBPC3(NM_000256.3):c.3065G>C (p.R1022P)
ISCN -
DB-ID MYBPC3_000261 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) 2.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
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.3065G>C r.(?) p.(Arg1022Pro)
MADD NM_003682.3 +?/. - c.*4532C>G r.(=) p.(=)


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