Overview

Variant ID 28642
Entrez Gene ID 7109
Gene TRAPPC10 (GeneCards)
Location hg19 21:45437249-45437249
hg38 21:44017368-44017368
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000021.8:g.45437249 G>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 48129895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.421
CADD Raw score (version 1.3) -0.384481 (Deleterious)
FATHMM raw prediction score 0.04921 (Tolerated)
Deleterious probability by DeFine 0.3387 (Neutral)
Entrez Gene ID 7109 (NCBI Gene)
Official Gene Symbol TRAPPC10 (GeneCards)
Number of variants in TRAPPC10 in this database 3 (view all the variants)
Full name trafficking protein particle complex 10
Band 21q22.3
Other IDs Vega: OTTHUMG00000086894
OMIM: 602103
HGNC: HGNC:11868
Ensembl: ENSG00000160218
Other names EHOC1, GT334, TMEM1, TRS30, EHOC-1, TRS130
Summary The protein encoded by this gene is a transmembrane protein found in the cis-Golgi complex. The encoded protein is part of the multisubunit transport protein particle (TRAPP) complex and may be involved in vesicular transport from the endoplasmic reticulum to the Golgi. Mutations in this gene could be responsible for the Unverricht-Lundborg type of progressive myoclonus epilepsy, or for autoimmune polyglandular disease type 1. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.02 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID