View genomic variant #0000021307

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.52942059G>C
Published as -
GERP -
Segregation -
DB-ID NDUFS4_000014
MSCV MSCV_0021307
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 0000021307 ./. - - c.178-4G>C p.? - - - -
NDUFS4 00000212 XM_005248525.1 0000021307 ./. - - c.178-4G>C p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000337873; RCV000395461; RCV002523527;
Chromosome 5:52942059..52942059
ClinVar Allele ID 304216
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Mitochondrial complex I deficiency, nuclear type 1|Leigh syndrome
HGVS variant names NC 000005.9:g.52942059G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA3264238
Gene symbol:Gene id. NDUFS4:4724
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 200384843
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