View genomic variant #0000023676

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.40309803G>A
Published as -
GERP -
Segregation -
DB-ID TRIT1_000002
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner Lishuang Shen




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
TRIT1 00003053 NM_017646.4 0000023676 ./. - - c.1204C>T p.(Arg402*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000477659; RCV000584729; RCV001755719;
Chromosome 1:40309803..40309803
Allele frequencies from ExAC 0.00002
Allele frequencies from TGP 0.00020
ClinVar Allele ID 404613
Disease database name and identifier MedGen:C3661900|MedGen:CN242004|MONDO:MONDO:0054742, MedGen:C4693466, OMIM:617873
ClinVar preferred disease name not provided|TRIT1 Deficiency|Combined oxidative phosphorylation deficiency 35
HGVS variant names NC 000001.10:g.40309803G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Pathogenic(1)|Uncertain significance(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA787882|OMIM:617840.0004
Gene symbol:Gene id. TRIT1:54802
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 367752391
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None