View genomic variant #0000000855

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) g.207638988C>T
Published as -
GERP 4.790
Segregation -
DB-ID FASTKD2_000001 See all 2 reported entries
MSCV MSCV_0000855
dbSNP ID rs118203917
Frequency -
Sources ; clinVar; Ensembl;
Reference 18771761
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 0000000855 +/+ - 7/12 c.1294C>T p.(Arg432*) - stop_gained - -
FASTKD2 00000128 NM_001136194.1 0000000855 +/+ - 7/12 c.1294C>T p.(Arg432*) - stop_gained - -
FASTKD2 00000130 NM_014929.3 0000000855 +/+ - 7/12 c.1294C>T p.? - stop_gained - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000000673; RCV001089468;
Chromosome 2:207638988..207638988
ClinVar Allele ID 15680
Disease database name and identifier MONDO:MONDO:0030020, MedGen:C5394293, OMIM:618855|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name Combined oxidative phosphorylation deficiency 44|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207638988C>T
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA114376|OMIM:612322.0001
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001587|nonsense
Allele origin germline
dbSNP ID 118203917
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