Variant #0000880885 (NC_000011.9:g.47369403C>T, NC_000011.9(NM_000256.3):c.821+5G>A (MYBPC3))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.47369403C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID MYBPC3_000339 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs397516077
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-10-19 14:30:01 +02:00 (CEST)
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.821+5G>A r.(?) p.(?)


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