View genomic variant #0000016445

Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.47602541G>T
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000013
MSCV MSCV_0016445
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 LOVD




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     
NDUFS3 00000211 NM_004551.2 0000016445 ./. - - c.381+5G>T p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000261462; RCV000352949;
Chromosome 11:47602541..47602541
ClinVar Allele ID 320898
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
HGVS variant names NC 000011.9:g.47602541G>T
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:CA10635057
Gene symbol:Gene id. NDUFS3:4722
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 886048392
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