View genomic variant #0000018222

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.12901770C>G
Published as -
GERP -
Segregation -
DB-ID ELAC2_000047
MSCV MSCV_0018222
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) 0.01 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 0000018222 ./. - - c.1359G>C p.(=) - - - -
ELAC2 00001871 NM_018127.6 0000018222 ./. - - c.1479G>C p.(=) - - - -
ELAC2 00001870 NM_173717.1 0000018222 ./. - - c.1476G>C p.(=) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000232716; RCV000438191; RCV003316292;
Chromosome 17:12901770..12901770
Allele frequencies from ESP 0.01000
Allele frequencies from TGP 0.00719
ClinVar Allele ID 242588
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913|MedGen:CN169374|MONDO:MONDO:0013872, MedGen:C3539120, OMIM:614731, Orphanet:1331
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17|not specified|Prostate cancer, hereditary, 2
HGVS variant names NC 000017.10:g.12901770C>G
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8401188
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 140335642
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000425836; RCV002062695;
Chromosome 17:12901770..12901770
ClinVar Allele ID 378060
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name not specified|Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12901770C>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA8401189
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001819|synonymous variant
Allele origin germline
dbSNP ID 140335642
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