View genomic variant #0000015592

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.161183429del
Published as -
GERP -
Segregation -
DB-ID NDUFS2_000015
MSCV MSCV_0015592
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

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 0000015592 ./. - - c.1213-10del p.(=) - - - -
NDUFS2 00000208 NM_004550.4 0000015592 ./. - - c.1213-10del p.(=) - - - -
NDUFS2 00000207 XM_005245208.1 0000015592 ./. - - c.1213-10del p.(=) - - - -
NDUFS2 00000210 XM_005245209.1 0000015592 ./. - - c.919-10del p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000400389;
Chromosome 1:161183429..161183429
ClinVar Allele ID 277989
Disease database name and identifier MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name Mitochondrial complex I deficiency
HGVS variant names NC 000001.10:g.161183430del
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Variant clinical sources reported ClinGen:CA1208819
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 750838845
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