Variant #0000540835 (NC_000010.10:g.75532101G>A, NM_004922.3:c.*1248G>A (SEC24C))

Chromosome 10
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.75532101G>A
DNA change (hg38) g.73772343G>A
Published as FUT11(NM_001284194.1):c.10G>A (p.G4S)
ISCN -
DB-ID FUT11_000002
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC24C NM_004922.3 -?/. - c.*1248G>A r.(=) p.(=)
FUT11 NM_173540.2 -?/. - c.10G>A r.(?) p.(Gly4Ser)


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