View genomic variant #0000019368

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207008821G>C
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000031
MSCV MSCV_0019368
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00031 View details
Owner LOVD




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 0000019368 ./. - - c.800C>G p.(Thr267Ser) - - - -
NDUFS1 00000202 NM_001199982.1 0000019368 ./. - - c.575C>G p.(Thr192Ser) - - - -
NDUFS1 00000203 NM_001199983.1 0000019368 ./. - - c.737C>G p.(Thr246Ser) - - - -
NDUFS1 00000206 NM_001199984.1 0000019368 ./. - - c.950C>G p.(Thr317Ser) - - - -
NDUFS1 00000205 NM_005006.6 0000019368 ./. - - c.908C>G p.(Thr303Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000477869; RCV002489139; RCV003105917;
Chromosome 2:207008821..207008821
Allele frequencies from ESP 0.00031
Allele frequencies from ExAC 0.00019
Allele frequencies from TGP 0.00040
ClinVar Allele ID 404755
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0100133, MedGen:C1838979, Orphanet:2609|MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226
ClinVar preferred disease name not provided|Mitochondrial complex I deficiency|Mitochondrial complex 1 deficiency, nuclear type 5
HGVS variant names NC 000002.11:g.207008821G>C
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
Variant clinical sources reported ClinGen:CA2070622
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 75666426
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