View genomic variant #0000004179

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.15884G>A
Published as -
GERP -2.530
Segregation -
DB-ID chrM_001148 See all 3 reported entries
MSCV MSCV_0004179
dbSNP ID rs28617642
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.
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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 0000004179 ?/? - . c.1138G>A p.A380T - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000133439; RCV000855397;
Chromosome M:15884..15884
ClinVar Allele ID 153625
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.15884G>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:CA170530
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 527236195
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000238892; RCV000855396;
Chromosome M:15884..15884
ClinVar Allele ID 247210
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not specified|Leigh syndrome
HGVS variant names NC 012920.1:m.15884G>C
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:CA10586049
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 527236195
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