Variant #0000544489 (NC_000011.9:g.47372988C>T, NM_000256.3:c.94G>A (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.47372988C>T
DNA change (hg38) g.47351437C>T
Published as MYBPC3(NM_000256.3):c.94G>A (p.E32K)
ISCN -
DB-ID MYBPC3_000444 See all 2 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) 0.00016 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 2019-12-04 15:24:38 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 +?/. - c.94G>A r.(?) p.(Glu32Lys)
SPI1 NM_003120.2 +?/. - c.*3790G>A r.(=) p.(=)


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