View genomic variant #0000021303

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.52856505T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS4_000005
MSCV MSCV_0021303
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

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

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS4 00000213 NM_002495.2 0000021303 ./. - - c.13T>C p.(Ser5Pro) - - - -
NDUFS4 00000212 XM_005248525.1 0000021303 ./. - - c.13T>C p.(Ser5Pro) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000198881; RCV000295911; RCV000329830; RCV000660466; RCV002517243;
Chromosome 5:52856505..52856505
Allele frequencies from ExAC 0.00021
ClinVar Allele ID 211157
Disease database name and identifier MedGen:CN517202|MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name not provided|Inborn genetic diseases|Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome|Mitochondrial complex I deficiency
HGVS variant names NC 000005.9:g.52856505T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(4)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA323413
Gene symbol:Gene id. NDUFS4:4724|LOC129993885:129993885
Molecular consequence SO:0001583|missense variant, SO:0001619|non-coding transcript variant
Allele origin
dbSNP ID 149323691
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