View genomic variant #0000019389

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.207630360C>T
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000065
MSCV MSCV_0019389
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 0000019389 ./. - - c.-162C>T p.(=) - - - -
FASTKD2 00000128 NM_001136194.1 0000019389 ./. - - c.-177C>T p.(=) - - - -
FASTKD2 00000130 NM_014929.3 0000019389 ./. - - c.-69C>T p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000124988; RCV000394368;
Chromosome 2:207630360..207630360
Allele frequencies from TGP 0.01038
ClinVar Allele ID 141000
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name not specified|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207630360C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA290853
Gene symbol:Gene id. FASTKD2:22868|LOC129935479:129935479
Molecular consequence SO:0001623|5 prime UTR variant
Allele origin germline
dbSNP ID 16838842
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