Variant #0000445524 (NC_000011.9:g.47354175C>T, NM_000256.3:c.3569G>A (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.47354175C>T
DNA change (hg38) g.47332624C>T
Published as -
ISCN -
DB-ID MYBPC3_000409 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs117354682
Origin Germline
Segregation -
Frequency T=0.003/1
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 4.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-11-01 13:37:12 +01:00 (CET)
Date last edited 2019-01-06 17:31:14 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYBPC3 NM_000256.3 ?/. 32 c.3569G>A r.(?) p.(Arg1190His)


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