View genomic variant #0000004142

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.15452C>A
Published as -
GERP -7.880
Segregation -
DB-ID chrM_000516 See all 3 reported entries
MSCV MSCV_0004142
dbSNP ID rs3088309
Frequency -
Sources ;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

1 entry on 1 page. Showing entry 1.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
MT-CYB 00001350 MT-CYB-201 0000004142 ?/? - . c.706C>A p.L236I - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000133456; RCV000855295;
Chromosome M:15452..15452
ClinVar Allele ID 153648
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|Human Phenotype Ontology:HP:0100615, MONDO:MONDO:0021068, MeSH:D010051, MedGen:C0919267, OMIM:167000
ClinVar preferred disease name Leigh syndrome|Neoplasm of ovary
HGVS variant names NC 012920.1:m.15452C>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:CA345759
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 193302994
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000855296;
Chromosome M:15452..15453
ClinVar Allele ID 680776
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leigh syndrome
HGVS variant names NC 012920.1:m.15452 15453delinsAC
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type Indel
Sequence Ontology for variant type SO:1000032
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 1603225292
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