View genomic variant #0000019358

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.206997706C>T
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000025
MSCV MSCV_0019358
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 0000019358 ./. - - c.1408G>A p.(Val470Ile) - - - -
NDUFS1 00000202 NM_001199982.1 0000019358 ./. - - c.1183G>A p.(Val395Ile) - - - -
NDUFS1 00000203 NM_001199983.1 0000019358 ./. - - c.1345G>A p.(Val449Ile) - - - -
NDUFS1 00000206 NM_001199984.1 0000019358 ./. - - c.1558G>A p.(Val520Ile) - - - -
NDUFS1 00000205 NM_005006.6 0000019358 ./. - - c.1516G>A p.(Val506Ile) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000348996; RCV000397471; RCV001728094; RCV002252098; RCV001861145;
Chromosome 2:206997706..206997706
Allele frequencies from ESP 0.00031
Allele frequencies from ExAC 0.00042
Allele frequencies from TGP 0.00040
ClinVar Allele ID 287237
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|.|MONDO:MONDO:0032610, MedGen:C4748754, OMIM:618226
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1|not provided|Leigh syndrome|See cases|Mitochondrial complex 1 deficiency, nuclear type 5
HGVS variant names NC 000002.11:g.206997706C>T
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(6)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2070426
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 137889316
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