View genomic variant #0000019401

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207638989G>A
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000076
MSCV MSCV_0019401
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00015 View details
Owner LOVD




Variant on transcripts

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

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 0000019401 ./. - - c.1295G>A p.(Arg432Gln) - - - -
FASTKD2 00000128 NM_001136194.1 0000019401 ./. - - c.1295G>A p.(Arg432Gln) - - - -
FASTKD2 00000130 NM_014929.3 0000019401 ./. - - c.1295G>A p.(Arg432Gln) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000199619; RCV000369329; RCV002515396;
Chromosome 2:207638989..207638989
Allele frequencies from ESP 0.00015
Allele frequencies from ExAC 0.00003
ClinVar Allele ID 210761
Disease database name and identifier MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905|MedGen:CN169374|MeSH:D030342, MedGen:C0950123
ClinVar preferred disease name Cytochrome-c oxidase deficiency disease|not specified|Inborn genetic diseases
HGVS variant names NC 000002.11:g.207638989G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA324157
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 372022584
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