View genomic variant #0000001351

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.3796A>G
Published as -
GERP -6.850
Segregation -
DB-ID chrM_000204 See all 2 reported entries
MSCV MSCV_0001351
dbSNP ID rs28357970
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 11938495;12756609
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 0000001351 +/+ - . c.490A>G p.T164A - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010382; RCV000853708; RCV000992363;
Chromosome M:3796..3796
ClinVar Allele ID 24769
Disease database name and identifier MedGen:CN517202|MedGen:C0752197|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Dystonia, adult-onset|Leigh syndrome
HGVS variant names NC 012920.1:m.3796A>G
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:CA340947|OMIM:516000.0011
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 28357970
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000224953; RCV000853709;
Chromosome M:3796..3796
ClinVar Allele ID 237334
Disease database name and identifier MedGen:CN517202|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name not provided|Leigh syndrome
HGVS variant names NC 012920.1:m.3796A>T
ClinVar review status criteria provided, multiple submitters, no conflicts
Clinical Significance Benign/Likely benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA10581388
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 28357970
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND1Adult-Onset DystoniaA3796GT-A-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None