View genomic variant #0000019356

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.206992622T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000009 See all 2 reported entries
MSCV MSCV_0000847
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
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 0000019356 ./. - - c.1675A>G p.(Thr559Ala) - - - -
NDUFS1 00000202 NM_001199982.1 0000019356 ./. - - c.1450A>G p.(Thr484Ala) - - - -
NDUFS1 00000203 NM_001199983.1 0000019356 ./. - - c.1612A>G p.(Thr538Ala) - - - -
NDUFS1 00000206 NM_001199984.1 0000019356 ./. - - c.1825A>G p.(Thr609Ala) - - - -
NDUFS1 00000205 NM_005006.6 0000019356 ./. - - c.1783A>G p.(Thr595Ala) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000024604; RCV001582499;
Chromosome 2:206992622..206992622
Allele frequencies from ExAC 0.00001
ClinVar Allele ID 40569
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.206992622T>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Likely pathogenic(1)|Uncertain significance(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA129896|OMIM:157655.0005
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 387907199
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