Variant #0000544497 (NC_000011.9:g.47374187C>T, NM_000256.3:c.12G>A (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47374187C>T
DNA change (hg38) g.47352636C>T
Published as MYBPC3(NM_000256.3):c.12G>A (p.P4=)
ISCN -
DB-ID MYBPC3_000448 See all 3 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) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-30 15:16:24 +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.12G>A r.(?) p.(Pro4=)
SPI1 NM_003120.2 -?/. - c.*2591G>A r.(=) p.(=)


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