Variant #0000929910 (NC_000011.9:g.47372440T>C, NC_000011.9(NM_000256.3):c.293-274A>G (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47372440T>C
DNA change (hg38) -
Published as MYBPC3(NM_000256.3):c.293-274A>G
ISCN -
DB-ID MYBPC3_001586
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 -/. - c.293-274A>G r.(=) p.(=)
SPI1 NM_003120.2 -/. - c.*4338A>G r.(=) p.(=)


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