Overview

Variant ID 11357
Entrez Gene ID 79783
Gene SUGCT (GeneCards)
Location hg19 7:40351778-40351778
hg38 7:40312179-40312179
Disease Cockayne syndrome (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000007.13:g.40351778 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 159138663

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.6445
CADD Raw score (version 1.3) -0.597258 (Deleterious)
FATHMM raw prediction score 0.05478 (Tolerated)
Deleterious probability by DeFine 0.1488 (Neutral)
Entrez Gene ID 79783 (NCBI Gene)
Official Gene Symbol SUGCT (GeneCards)
Number of variants in SUGCT in this database 8 (view all the variants)
Full name succinyl-CoA:glutarate-CoA transferase
Band 7p14.1
Other IDs Vega: OTTHUMG00000155094
OMIM: 609187
HGNC: HGNC:16001
Ensembl: ENSG00000175600
Other names GA3, ORF19, DERP13, C7orf10
Summary This gene encodes a protein that is similar to members of the CaiB/baiF CoA-transferase protein family. Mutations in this gene are associated with glutaric aciduria type III. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2010]

Individual #1

Individual ID 29217584.16 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Cockayne syndrome (view all the variants in this disease)
OMIM ID 216400

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;