View genomic variant #0000018198

Chromosome 17
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.12896263G>A
Published as -
GERP -
Segregation -
DB-ID ELAC2_000024
MSCV MSCV_0018198
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     
ELAC2 00001869 NM_001165962.1 0000018198 ./. - - c.2233C>T p.(Arg745Trp) - - - -
ELAC2 00001871 NM_018127.6 0000018198 ./. - - c.2353C>T p.(Arg785Trp) - - - -
ELAC2 00001870 NM_173717.1 0000018198 ./. - - c.2350C>T p.(Arg784Trp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000465852; RCV000786309;
Chromosome 17:12896263..12896263
ClinVar Allele ID 401538
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913|MedGen:CN517202
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17|not provided
HGVS variant names NC 000017.10:g.12896263G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA16615097
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 1060502162
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