View genomic variant #0000019423

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207657741G>A
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000011
MSCV MSCV_0019423
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

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 0000019423 ./. - - c.*1215G>A p.(=) - - - -
FASTKD2 00000128 NM_001136194.1 0000019423 ./. - - c.*1215G>A p.(=) - - - -
FASTKD2 00000130 NM_014929.3 0000019423 ./. - - c.*1215G>A p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000324665;
Chromosome 2:207657741..207657741
Allele frequencies from TGP 0.18530
ClinVar Allele ID 286901
Disease database name and identifier MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207657741G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10613733
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001624|3 prime UTR variant
Allele origin germline
dbSNP ID 111954117
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