View genomic variant #0000016439

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.47600603T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000016
MSCV MSCV_0016439
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.
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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 0000016439 ./. - - c.-41T>C p.(=) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000290487; RCV000347926;
Chromosome 11:47600603..47600603
Allele frequencies from ExAC 0.00000
ClinVar Allele ID 314314
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial complex I deficiency|Leigh syndrome
HGVS variant names NC 000011.9:g.47600603T>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:CA5977754
Gene symbol:Gene id. NDUFS3:4722
Allele origin germline
dbSNP ID 750965789
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