View genomic variant #0000001505

Chromosome M
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.14831G>A
Published as -
GERP -8.300
Segregation -
DB-ID chrM_000042 See all 3 reported entries
MSCV MSCV_0001505
dbSNP ID rs199795644
Frequency -
Sources ; clinVar; Mitomap; ensembl;
Reference 20301353
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 0000001505 +/+ - . c.85G>A p.A29T - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000055706; RCV000855165;
Chromosome M:14831..14831
ClinVar Allele ID 76425
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104
ClinVar preferred disease name Leigh syndrome|Leber optic atrophy
HGVS variant names NC 012920.1:m.14831G>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:CA344826
Gene symbol:Gene id. MT-CYB:4519
Allele origin
dbSNP ID 199795644
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000855164;
Chromosome M:14831..14831
ClinVar Allele ID 680663
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.14831G>C
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 199795644
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBLHONG14831AA-T+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None