View genomic variant #0000015589

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.161180512A>G
Published as -
GERP -
Segregation -
DB-ID NDUFS2_000012
MSCV MSCV_0015589
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02014 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 0000015589 ./. - - c.986+12A>G p.(=) - - - -
NDUFS2 00000208 NM_004550.4 0000015589 ./. - - c.986+12A>G p.(=) - - - -
NDUFS2 00000207 XM_005245208.1 0000015589 ./. - - c.986+12A>G p.(=) - - - -
NDUFS2 00000210 XM_005245209.1 0000015589 ./. - - c.692+12A>G p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000127151; RCV000397312; RCV002055707; RCV003343653;
Chromosome 1:161180512..161180512
Allele frequencies from ESP 0.02014
Allele frequencies from ExAC 0.00570
Allele frequencies from TGP 0.01238
ClinVar Allele ID 142189
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MONDO:MONDO:0032611, MedGen:C4748759, OMIM:618228|MedGen:CN169374|MedGen:C3661900
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1|Mitochondrial complex 1 deficiency, nuclear type 6|not specified|not provided
HGVS variant names NC 000001.10:g.161180512A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA292497
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 11265565
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