View genomic variant #0000019396

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.207631944C>T
Published as -
GERP -
Segregation -
DB-ID FASTKD2_000072
MSCV MSCV_0019396
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 0000019396 ./. - - c.527C>T p.(Ala176Val) - - - -
FASTKD2 00000128 NM_001136194.1 0000019396 ./. - - c.527C>T p.(Ala176Val) - - - -
FASTKD2 00000130 NM_014929.3 0000019396 ./. - - c.527C>T p.(Ala176Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000299615; RCV001559445;
Chromosome 2:207631944..207631944
Allele frequencies from ExAC 0.00004
Allele frequencies from TGP 0.00020
ClinVar Allele ID 286880
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0009068, MedGen:C5435656, OMIM:220110, Orphanet:254905
ClinVar preferred disease name not provided|Cytochrome-c oxidase deficiency disease
HGVS variant names NC 000002.11:g.207631944C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA2074894
Gene symbol:Gene id. FASTKD2:22868
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 367909050
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