View genomic variant #0000001356

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.4136A>G
Published as -
GERP 4.530
Segregation -
DB-ID chrM_000001 See all 2 reported entries
MSCV MSCV_0001356
dbSNP ID rs199476121
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 1928099
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 0000001356 +/+ - . c.830A>G p.T277C - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010378; RCV000853739;
Chromosome M:4136..4136
ClinVar Allele ID 24766
Disease database name and identifier Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Leber optic atrophy|Leigh syndrome
HGVS variant names NC 012920.1:m.4136A>G
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:CA254860|OMIM:516000.0006
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 199476121
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND1LHONA4136GY-C+-Possibly synergisticCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None