Variant #0000612638 (NC_000010.10:g.75529666C>T, NM_004922.3:c.2755C>T (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.75529666C>T
DNA change (hg38) g.73769908C>T
Published as SEC24C(NM_004922.4):c.2755C>T (p.P919S)
ISCN -
DB-ID FUT11_000004
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEC24C NM_004922.3 ?/. - c.2755C>T r.(?) p.(Pro919Ser)
FUT11 NM_173540.2 ?/. - c.-2426C>T r.(?) p.(=)


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