View genomic variant #0000015596

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.161183716G>A
Published as -
GERP -
Segregation -
DB-ID NDUFS2_000018
MSCV MSCV_0015596
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00038 View details
Owner LOVD




Variant on transcripts

4 entries on 1 page. Showing entries 1 - 4.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS2 00000209 NM_001166159.1 0000015596 ./. - - c.1359G>A p.(=) - - - -
NDUFS2 00000208 NM_004550.4 0000015596 ./. - - c.1354+5G>A p.? - - - -
NDUFS2 00000207 XM_005245208.1 0000015596 ./. - - c.1354+5G>A p.? - - - -
NDUFS2 00000210 XM_005245209.1 0000015596 ./. - - c.1060+5G>A p.? - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000127152; RCV000275644; RCV001303885;
Chromosome 1:161183716..161183716
Allele frequencies from ESP 0.00038
Allele frequencies from ExAC 0.00026
Allele frequencies from TGP 0.00020
ClinVar Allele ID 142190
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:CN169374
ClinVar preferred disease name not provided|Mitochondrial complex I deficiency, nuclear type 1|not specified
HGVS variant names NC 000001.10:g.161183716G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(3)|Benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA292498
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001627|intron variant, SO:0001819|synonymous variant
Allele origin
dbSNP ID 190184430
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