View genomic variant #0000025781

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.206988964C>T
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000056
MSCV -
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 Lishuang Shen




Variant on transcripts

5 entries on 1 page. Showing entries 1 - 5.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFS1 00000204 NM_001199981.1 0000025781 ./. - - c.2021G>A p.(Cys674Tyr) - - - -
NDUFS1 00000202 NM_001199982.1 0000025781 ./. - - c.1796G>A p.(Cys599Tyr) - - - -
NDUFS1 00000203 NM_001199983.1 0000025781 ./. - - c.1958G>A p.(Cys653Tyr) - - - -
NDUFS1 00000206 NM_001199984.1 0000025781 ./. - - c.2171G>A p.(Cys724Tyr) - - - -
NDUFS1 00000205 NM_005006.6 0000025781 ./. - - c.2129G>A p.(Cys710Tyr) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000680046; RCV003153798;
Chromosome 2:206988964..206988964
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 552061
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609
ClinVar preferred disease name not provided|Mitochondrial complex I deficiency
HGVS variant names NC 000002.11:g.206988964C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin
dbSNP ID 765677840
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