View genomic variant #0000019382

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207017173G>A
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000041
MSCV MSCV_0019382
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.02845 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 0000019382 ./. - - c.123C>T p.(=) - - - -
NDUFS1 00000202 NM_001199982.1 0000019382 ./. - - c.5+1169C>T p.(=) - - - -
NDUFS1 00000203 NM_001199983.1 0000019382 ./. - - c.-19+1169C>T p.(=) - - - -
NDUFS1 00000206 NM_001199984.1 0000019382 ./. - - c.165C>T p.(=) - - - -
NDUFS1 00000205 NM_005006.6 0000019382 ./. - - c.123C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000127147; RCV000275731; RCV000386489; RCV002055704;
Chromosome 2:207017173..207017173
Allele frequencies from ESP 0.02845
Allele frequencies from ExAC 0.00744
Allele frequencies from TGP 0.02656
ClinVar Allele ID 142185
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010
ClinVar preferred disease name not specified|not provided|Leigh syndrome|Mitochondrial complex I deficiency, nuclear type 1
HGVS variant names NC 000002.11:g.207017173G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA292492
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001627|intron variant, SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 2230888
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