View genomic variant #0000025786

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.207011681A>G
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000055
MSCV -
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
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 0000025786 ./. - - c.575T>C p.(Val192Ala) - - - -
NDUFS1 00000202 NM_001199982.1 0000025786 ./. - - c.350T>C p.(Val117Ala) - - - -
NDUFS1 00000203 NM_001199983.1 0000025786 ./. - - c.512T>C p.(Val171Ala) - - - -
NDUFS1 00000206 NM_001199984.1 0000025786 ./. - - c.725T>C p.(Val242Ala) - - - -
NDUFS1 00000205 NM_005006.6 0000025786 ./. - - c.683T>C p.(Val228Ala) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000493658; RCV000779296;
Chromosome 2:207011681..207011681
Allele frequencies from ESP 0.00023
Allele frequencies from ExAC 0.00006
ClinVar Allele ID 421356
Disease database name and identifier MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226|MedGen:C3661900
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 5|not provided
HGVS variant names NC 000002.11:g.207011681A>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Pathogenic/Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2070700
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 370411488
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