View genomic variant #0000019357

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.206994851G>A
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000001 See all 2 reported entries
MSCV MSCV_0000848
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 8.0E-5 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 0000019357 ./. - - c.1561C>T p.(Arg521*) - - - -
NDUFS1 00000202 NM_001199982.1 0000019357 ./. - - c.1336C>T p.(Arg446*) - - - -
NDUFS1 00000203 NM_001199983.1 0000019357 ./. - - c.1498C>T p.(Arg500*) - - - -
NDUFS1 00000206 NM_001199984.1 0000019357 ./. - - c.1711C>T p.(Arg571*) - - - -
NDUFS1 00000205 NM_005006.6 0000019357 ./. - - c.1669C>T p.(Arg557*) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000043635; RCV001558587;
Chromosome 2:206994851..206994851
Allele frequencies from ESP 0.00008
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 65582
Disease database name and identifier MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226|MedGen:CN517202
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 5|not provided
HGVS variant names NC 000002.11:g.206994851G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA143871|OMIM:157655.0007
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001587|nonsense
Allele origin
dbSNP ID 372691318
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