View genomic variant #0000018192

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.12896200_12896201insATCCTCCAGGCCGCCTGCCAGCTCCCTGGACAGGAGGGCCGCCCGCACCTGCCGCAGCCCCCG
Published as -
GERP -
Segregation -
DB-ID ELAC2_000061
MSCV MSCV_0018192
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 0000018192 ./. - - c.2295_2296insCGGGGGCTGCGGCAGGTGCGGGCGGCCCTCCTGTCCAGGGAGCTGGCAGGCGGCCTGGAGGAT p.(Asp765_Gly766insArgGlyLeuArgGlnValArgAlaAlaLeuLeuSerArgGluLeuAlaGlyGlyLeuGluAsp) - - - -
ELAC2 00001871 NM_018127.6 0000018192 ./. - - c.2415_2416insCGGGGGCTGCGGCAGGTGCGGGCGGCCCTCCTGTCCAGGGAGCTGGCAGGCGGCCTGGAGGAT p.(Asp805_Gly806insArgGlyLeuArgGlnValArgAlaAlaLeuLeuSerArgGluLeuAlaGlyGlyLeuGluAsp) - - - -
ELAC2 00001870 NM_173717.1 0000018192 ./. - - c.2412_2413insCGGGGGCTGCGGCAGGTGCGGGCGGCCCTCCTGTCCAGGGAGCTGGCAGGCGGCCTGGAGGAT p.(Asp804_Gly805insArgGlyLeuArgGlnValArgAlaAlaLeuLeuSerArgGluLeuAlaGlyGlyLeuGluAsp) - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000233736;
Chromosome 17:12896200..12896201
ClinVar Allele ID 242582
Disease database name and identifier MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12896258 12896259insCCCCGATCCTCCAGGCCGCCTGCCAGCTCCCTGGACAGGAGGGCCGCCCGCACCTGCCGCAGC
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Insertion
Sequence Ontology for variant type SO:0000667
Variant clinical sources reported ClinGen:CA10583446
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 878855051
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000460318; RCV002526419;
Chromosome 17:12896200..12896201
ClinVar Allele ID 401537
Disease database name and identifier MeSH:D030342, MedGen:C0950123|MONDO:MONDO:0014190, MedGen:C3809526, OMIM:615440, Orphanet:369913
ClinVar preferred disease name Inborn genetic diseases|Combined oxidative phosphorylation defect type 17
HGVS variant names NC 000017.10:g.12896201 12896263dup
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Uncertain significance
Variant type Duplication
Sequence Ontology for variant type SO:1000035
Variant clinical sources reported ClinGen:CA8400800
Gene symbol:Gene id. ELAC2:60528
Molecular consequence SO:0001821|inframe insertion
Allele origin germline
dbSNP ID 1555571246
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