View genomic variant #0000004590

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.4769A>G
Published as -
GERP -8.800
Segregation -
DB-ID chrM_001074 See all 2 reported entries
MSCV MSCV_0004590
dbSNP ID rs3021086
Frequency -
Sources ; Mitomap;
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-ND2 00001325 MT-ND2-201 0000004590 +?/+? - . c.300A>G p.M100M - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000509491; RCV002221548;
Chromosome M:4769..4769
ClinVar Allele ID 434779
Disease database name and identifier MedGen:C3661900|MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380
ClinVar preferred disease name not provided|Mitochondrial disease
HGVS variant names NC 012920.1:m.4769A>G
ClinVar review status reviewed by expert panel
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA337096951
Gene symbol:Gene id. MT-ND2:4536
Allele origin germline
dbSNP ID 3021086
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND2SZ-associatedA4769Asyn+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None