Variant #0000979388 (NC_000011.9:g.118889889T>G, NM_016146.4:c.212T>G (TRAPPC4))

Chromosome 11
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.118889889T>G
DNA change (hg38) -
Published as TRAPPC4(NM_016146.6):c.212T>G (p.(Val71Gly))
ISCN -
DB-ID CCDC84_000003
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_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     
RPS25 NM_001028.2 ?/. - c.-895A>C r.(?) p.(=)
TRAPPC4 NM_016146.4 ?/. - c.212T>G r.(?) p.(Val71Gly)
CCDC84 NM_198489.1 ?/. - c.*3581T>G r.(=) p.(=)


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