View genomic variant #0000023679

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.40313300A>C
Published as -
GERP -
Segregation -
DB-ID TRIT1_000005
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.
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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 0000023679 ./. - - c.848T>G p.(Ile283Ser) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000477657; RCV000584739; RCV002285336;
Chromosome 1:40313300..40313300
ClinVar Allele ID 404615
Disease database name and identifier MONDO:MONDO:0054742, MedGen:C4693466, OMIM:617873|MedGen:CN517202|MedGen:CN242004
ClinVar preferred disease name Combined oxidative phosphorylation deficiency 35|not provided|TRIT1 Deficiency
HGVS variant names NC 000001.10:g.40313300A>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA787986|OMIM:617840.0003
Gene symbol:Gene id. TRIT1:54802
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 199622789
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