View genomic variant #0000023678

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.40313292T>C
Published as -
GERP -
Segregation -
DB-ID TRIT1_000004
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 0000023678 ./. - - c.856A>G p.(Lys286Glu) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000477660; RCV000584735;
Chromosome 1:40313292..40313292
ClinVar Allele ID 404614
Disease database name and identifier MedGen:CN242004|MONDO:MONDO:0054742, MedGen:C4693466, OMIM:617873
ClinVar preferred disease name TRIT1 Deficiency|Combined oxidative phosphorylation deficiency 35
HGVS variant names NC 000001.10:g.40313292T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16616851|OMIM:617840.0005
Gene symbol:Gene id. TRIT1:54802
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 1060505019
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