Variant #0000805174 (NC_000011.9:g.47372949C>T, NM_000256.3:c.133G>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.47372949C>T
DNA change (hg38) -
Published as MYBPC3(NM_000256.3):c.133G>A (p.G45R)
ISCN -
DB-ID MYBPC3_000949 See all 2 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +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.133G>A r.(?) p.(Gly45Arg)
SPI1 NM_003120.2 ?/. - c.*3829G>A r.(=) p.(=)


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