Variant #0000889969 (NC_000011.9:g.47374188G>A, NM_000256.3:c.11C>T (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.47374188G>A
DNA change (hg38) -
Published as MYBPC3(NM_000256.3):c.11C>T (p.P4L)
ISCN -
DB-ID MYBPC3_001490
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 ?/. - c.11C>T r.(?) p.(Pro4Leu)
SPI1 NM_003120.2 ?/. - c.*2590C>T r.(=) p.(=)


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