View genomic variant #0000025784

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.207009643T>C
Published as -
GERP -
Segregation -
DB-ID NDUFS1_000053
MSCV -
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 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 0000025784 ./. - - c.737A>G p.(Asn246Ser) - - - -
NDUFS1 00000202 NM_001199982.1 0000025784 ./. - - c.512A>G p.(Asn171Ser) - - - -
NDUFS1 00000203 NM_001199983.1 0000025784 ./. - - c.674A>G p.(Asn225Ser) - - - -
NDUFS1 00000206 NM_001199984.1 0000025784 ./. - - c.887A>G p.(Asn296Ser) - - - -
NDUFS1 00000205 NM_005006.6 0000025784 ./. - - c.845A>G p.(Asn282Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000768439;
Chromosome 2:207009643..207009643
ClinVar Allele ID 614598
Disease database name and identifier MONDO:MONDO:0100224, MedGen:CN257533, OMIM:252010
ClinVar preferred disease name Mitochondrial complex I deficiency, nuclear type 1
HGVS variant names NC 000002.11:g.207009643T>C
ClinVar review status no assertion criteria provided
Clinical Significance Likely pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. NDUFS1:4719
Molecular consequence SO:0001583|missense variant
Allele origin inherited
dbSNP ID 1485032272
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