View genomic variant #0000023680

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.40349142G>A
Published as -
GERP -
Segregation -
DB-ID TRIT1_000006
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 0000023680 ./. - - c.22C>T p.(Arg8*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000477658; RCV000584740; RCV001796068; RCV002526505;
Chromosome 1:40349142..40349142
Allele frequencies from ExAC 0.00015
ClinVar Allele ID 404616
Disease database name and identifier MedGen:CN242004|MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0054742, MedGen:C4693466, OMIM:617873|MedGen:CN517202
ClinVar preferred disease name TRIT1 Deficiency|Inborn genetic diseases|Combined oxidative phosphorylation deficiency 35|not provided
HGVS variant names NC 000001.10:g.40349142G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA788227|OMIM:617840.0006
Gene symbol:Gene id. TRIT1:54802|MYCL-AS1:105378668
Molecular consequence SO:0001587|nonsense, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 184469579
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001763472;
Chromosome 1:40349142..40349142
Allele frequencies from ESP 0.00008
ClinVar Allele ID 1296182
Disease database name and identifier MedGen:C3661900
ClinVar preferred disease name not provided
HGVS variant names NC 000001.10:g.40349142G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. TRIT1:54802|MYCL-AS1:105378668
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin germline
dbSNP ID 184469579
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