View genomic variant #0000004475

Chromosome M
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.3565A>G
Published as -
GERP -5.210
Segregation -
DB-ID chrM_000695
MSCV MSCV_0004475
dbSNP ID rs2854133
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-ND1 00001321 MT-ND1-201 0000004475 ?/? - . c.259A>G p.T87A - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000853677;
Chromosome M:3565..3565
ClinVar Allele ID 680907
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.3565A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 2854133
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000853680;
Chromosome M:3566..3566
ClinVar Allele ID 680908
Disease database name and identifier MONDO:MONDO:0010780, MedGen:C3151898, OMIM:500009, Orphanet:254864
ClinVar preferred disease name Mitochondrial myopathy with reversible cytochrome C oxidase deficiency
HGVS variant names NC 012920.1:m.3571del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely pathogenic
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 1603219020
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