Variant #0000984002 (NC_000021.8:g.45518308G>A, NM_003274.4:c.3239G>A (TRAPPC10))

Chromosome 21
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.45518308G>A
DNA change (hg38) -
Published as TRAPPC10(NM_003274.5):c.3239G>A (p.(Cys1080Tyr))
ISCN -
DB-ID TRAPPC10_000010
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) 0.00018 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TRAPPC10 NM_003274.4 ?/. - c.3239G>A r.(?) p.(Cys1080Tyr)


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