Variant #0000719716 (NC_000004.11:g.119652605G>A, NM_014822.2:c.2734C>T (SEC24D))

Chromosome 4
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.119652605G>A
DNA change (hg38) -
Published as SEC24D(NM_001318066.1):c.2737C>T (p.R913C), SEC24D(NM_014822.2):c.2734C>T (p.(Arg912Cys))
ISCN -
DB-ID SEC24D_000036 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) 0.00037 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 2021-02-08 18:36:18 +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     
SEC24D NM_014822.2 ?/. - c.2734C>T r.(?) p.(Arg912Cys)


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