View genomic variant #0000001458

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.10398A>G
Published as -
GERP -10.300
Segregation -
DB-ID chrM_000075 See all 2 reported entries
MSCV MSCV_0001458
dbSNP ID rs2853826
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 17066297;6343397
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-ND3 00001340 MT-ND3-201 0000001458 +/+ - . c.340A>G p.T114A - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010359; RCV000854647;
Chromosome M:10398..10398
ClinVar Allele ID 24752
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MedGen:C4016597
ClinVar preferred disease name Leigh syndrome|Parkinson disease, resistance to
HGVS variant names NC 012920.1:m.10398A>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:CA120638|OMIM:516002.0002
Gene symbol:Gene id. MT-ND3:4537
Allele origin germline
dbSNP ID 2853826
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000854648;
Chromosome M:10398..10398
ClinVar Allele ID 680178
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.10398A>T
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ND3:4537
Allele origin germline
dbSNP ID 2853826
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND3Invasive Breast Cancer risk factor; AD; PD; BD lithium response; Type 2 DMA10398AT-T+-Reported; haplogroup HNTUVWXK2 markerCoding_and_Control_Region
MT-ND3PD protective factor/longevity/altered cell pH/metabolic syndrome/breast cancer riskA10398GT-A+-Reported; haplogroup IJK markerCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None