View genomic variant #0000015602

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.161184089_161184090insTA
Published as -
GERP -
Segregation -
DB-ID NDUFS2_000004
MSCV MSCV_0015602
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 0000015602 ./. - - c.*358_*359insTA p.(=) - - - -
NDUFS2 00000208 NM_004550.4 0000015602 ./. - - c.*106_*107insTA p.(=) - - - -
NDUFS2 00000207 XM_005245208.1 0000015602 ./. - - c.*106_*107insTA p.(=) - - - -
NDUFS2 00000210 XM_005245209.1 0000015602 ./. - - c.*106_*107insTA p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000267579;
Chromosome 1:161184089..161184090
ClinVar Allele ID 277894
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.161184091 161184092dup
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA10608521
Gene symbol:Gene id. NDUFS2:4720
Molecular consequence SO:0001619|non-coding transcript variant, SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 886045468
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