Variant #0000979137 (NC_000010.10:g.75532152G>A, NM_004922.3:c.*1299G>A (SEC24C))

Chromosome 10
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.75532152G>A
DNA change (hg38) -
Published as FUT11(NM_173540.3):c.61G>A (p.(Ala21Thr))
ISCN -
DB-ID FUT11_000005
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) 0.00083 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
SEC24C NM_004922.3 ?/. - c.*1299G>A r.(=) p.(=)
FUT11 NM_173540.2 ?/. - c.61G>A r.(?) p.(Ala21Thr)


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