View genomic variant #0000019399

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.207636605G>C
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000075
MSCV MSCV_0019399
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 0000019399 ./. - - c.991-13G>C p.(=) - - - -
FASTKD2 00000128 NM_001136194.1 0000019399 ./. - - c.991-13G>C p.(=) - - - -
FASTKD2 00000130 NM_014929.3 0000019399 ./. - - c.991-13G>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124986; RCV001139105; RCV001523313;
Chromosome 2:207636605..207636605
Allele frequencies from ESP 0.01473
Allele frequencies from TGP 0.01597
ClinVar Allele ID 140998
Disease database name and identifier MedGen:CN169374|MedGen:C3661900|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name not specified|not provided|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207636605G>A
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA290851
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 13421046
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000333402; RCV000606076; RCV002057639;
Chromosome 2:207636605..207636605
ClinVar Allele ID 284196
Disease database name and identifier MedGen:CN169374|MedGen:CN517202|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name not specified|not provided|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207636605G>C
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(1)|Likely benign(2)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2075033
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001627|intron variant
Allele origin germline
dbSNP ID 13421046
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