View genomic variant #0000018241

Chromosome 17
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.12920199G>A
Published as -
GERP -
Segregation -
DB-ID ELAC2_000022
MSCV MSCV_0018241
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.00023 View details
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     
ELAC2 00001869 NM_001165962.1 0000018241 ./. - - c.347C>T p.(Ser116Phe) - - - -
ELAC2 00001871 NM_018127.6 0000018241 ./. - - c.347C>T p.(Ser116Phe) - - - -
ELAC2 00001870 NM_173717.1 0000018241 ./. - - c.347C>T p.(Ser116Phe) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000462214; RCV001856810;
Chromosome 17:12920199..12920199
Allele frequencies from ESP 0.00023
Allele frequencies from ExAC 0.00033
Allele frequencies from TGP 0.00180
ClinVar Allele ID 401999
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913|MedGen:C3661900
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17|not provided
HGVS variant names NC 000017.10:g.12920199G>A
ClinVar review status criteria provided, conflicting interpretations
Clinical Significance Conflicting interpretations of pathogenicity
Conflicting clinical significance Uncertain significance(2)|Likely benign(1)
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8401716
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 140665334
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