View genomic variant #0000018211

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.12898323T>A
Published as -
GERP -
Segregation -
DB-ID ELAC2_000037
MSCV MSCV_0018211
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 0000018211 ./. - - c.1745A>T p.(Glu582Val) - - - -
ELAC2 00001871 NM_018127.6 0000018211 ./. - - c.1865A>T p.(Glu622Val) - - - -
ELAC2 00001870 NM_173717.1 0000018211 ./. - - c.1862A>T p.(Glu621Val) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000005362; RCV000230766;
Chromosome 17:12898323..12898323
Allele frequencies from TGP 0.00020
ClinVar Allele ID 20098
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913|MONDO:MONDO:0013872, MedGen:C3539120, OMIM:614731, Orphanet:1331
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17|Prostate cancer, hereditary, 2
HGVS variant names NC 000017.10:g.12898323T>A
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA117236|OMIM:605367.0005|UniProtKB:Q9BQ52#VAR 017429
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 119484087
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV001904552; RCV002489990;
Chromosome 17:12898323..12898323
ClinVar Allele ID 1473662
Disease database name and identifier MONDO:MONDO:0013872, MedGen:C3539120, OMIM:614731, Orphanet:1331|MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name Prostate cancer, hereditary, 2|Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12898323T>C
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
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001583|missense variant
Allele origin germline
dbSNP ID 119484087
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