View genomic variant #0000016444

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.47602147C>G
Published as -
GERP -
Segregation -
DB-ID NDUFS3_000012
MSCV MSCV_0016444
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 0000016444 ./. - - c.204C>G p.(Ile68Met) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000293525;
Chromosome 11:47602147..47602147
ClinVar Allele ID 275552
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name Leigh syndrome|Mitochondrial complex I deficiency
HGVS variant names NC 000011.9:g.47602147C>G
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:CA10607103
Gene symbol:Gene id. NDUFS3:4722
Molecular consequence SO:0001583|missense variant
Allele origin paternal
dbSNP ID 886044765
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