Variant #0000544051 (NC_000011.9:g.47353445_47353447del, NC_000011.9(NM_000256.3):c.3815-11_3815-9del (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47353445_47353447del
DNA change (hg38) g.47331894_47331896del
Published as -
ISCN -
DB-ID MADD_000017 See all 3 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) Retrieve
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 2020-08-06 14:59:34 +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 -?/. - c.3815-11_3815-9del r.(=) p.(=)
MADD NM_003682.3 -?/. - c.*2744_*2746del r.(=) p.(=)


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