View genomic variant #0000023512

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.119005896G>C
Published as -
GERP -
Segregation -
DB-ID NDUFA1_000003 See all 2 reported entries
MSCV MSCV_0001542
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

1 entry on 1 page. Showing entry 1.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
NDUFA1 00000182 NM_004541.3 0000023512 ./. - - c.22G>C p.(Gly8Arg) - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000012414;
Chromosome X:119005896..119005896
ClinVar Allele ID 26687
Disease database name and identifier MONDO:MONDO:0026720, MedGen:C4746984, OMIM:301020
ClinVar preferred disease name Mitochondrial complex 1 deficiency, nuclear type 12
HGVS variant names NC 000023.10:g.119005896G>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA121629|OMIM:300078.0001|UniProtKB:O15239#VAR 035099
Gene symbol:Gene id. NDUFA1:4694|LOC130068621:130068621
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 104894884
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