View genomic variant #0000015585

Chromosome 1
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.161179733_161179734insCCGG
Published as -
GERP -
Segregation -
DB-ID NDUFS2_000008
MSCV MSCV_0015585
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00048 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 0000015585 ./. - - c.702+12_702+13insCCGG p.(=) - - - -
NDUFS2 00000208 NM_004550.4 0000015585 ./. - - c.702+12_702+13insCCGG p.(=) - - - -
NDUFS2 00000207 XM_005245208.1 0000015585 ./. - - c.702+12_702+13insCCGG p.(=) - - - -
NDUFS2 00000210 XM_005245209.1 0000015585 ./. - - c.408+12_408+13insCCGG p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000343322; RCV000480470; RCV002059342;
Chromosome 1:161179733..161179734
ClinVar Allele ID 277975
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MedGen:CN517202
ClinVar preferred disease name not specified|Mitochondrial complex I deficiency|not provided
HGVS variant names NC 000001.10:g.161179735 161179738dup
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Benign(1)|Likely benign(1)
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA1208654
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 776704187
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