View genomic variant #0000019334

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.201943669T>C
Published as -
GERP -
Segregation -
DB-ID NDUFB3_000002
MSCV MSCV_0019334
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00123 View details
Owner LOVD




Variant on transcripts

2 entries on 1 page. Showing entries 1 - 2.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFB3 00000196 NM_001257102.1 0000019334 ./. - - c.64T>C p.(Trp22Arg) - - - -
NDUFB3 00000197 NM_002491.2 0000019334 ./. - - c.64T>C p.(Trp22Arg) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000239318; RCV000624796; RCV000504444; RCV000735413;
Chromosome 2:201943669..201943669
Allele frequencies from ESP 0.00123
Allele frequencies from ExAC 0.00067
Allele frequencies from TGP 0.00040
ClinVar Allele ID 246907
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MedGen:C3661900|MONDO:MONDO:0032629, MedGen:C4748806, OMIM:618246|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name Inborn genetic diseases|not provided|Mitochondrial complex 1 deficiency, nuclear type 25|Mitochondrial complex I deficiency
HGVS variant names NC 000002.11:g.201943669T>C
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:CA2052282|OMIM:603839.0001
Gene symbol:Gene id. NDUFB3:4709
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 142609245
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