Variant #0000445529 (NC_000011.9:g.47354270_47354294del, NC_000011.9(NM_000256.3):c.3491-41_3491-17del (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.47354270_47354294del
DNA change (hg38) g.47332719_47332743del
Published as -
ISCN -
DB-ID MYBPC3_000297 See all 5 reported entries
Variant remarks -
Reference PubMed: Waldmuller 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-12-31 16:29:42 +01:00 (CET)
Date last edited 2020-07-14 21:57:48 +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 +/. 31i c.3491-41_3491-17del r.3491_3627del p.Gly1164Alafs*


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