View genomic variant #0000019405

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.207656411A>G
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000052
MSCV MSCV_0019405
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00131 View details
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
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Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
FASTKD2 00000129 NM_001136193.1 0000019405 ./. - - c.2018A>G p.(Asn673Ser) - - - -
FASTKD2 00000128 NM_001136194.1 0000019405 ./. - - c.2018A>G p.(Asn673Ser) - - - -
FASTKD2 00000130 NM_014929.3 0000019405 ./. - - c.2018A>G p.(Asn673Ser) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000289795; RCV000676953; RCV002521366;
Chromosome 2:207656411..207656411
Allele frequencies from ESP 0.00131
Allele frequencies from ExAC 0.00111
Allele frequencies from TGP 0.00120
ClinVar Allele ID 284960
Disease database name and identifier MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MeSH:D030342, MedGen:C0950123|MedGen:C3661900
ClinVar preferred disease name Cytochrome-c oxidase deficiency disease|Inborn genetic diseases|not provided
HGVS variant names NC 000002.11:g.207656411A>G
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(3)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2075354
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 142211558
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