View genomic variant #0000003671

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.10084T>C
Published as -
GERP -1.980
Segregation -
DB-ID chrM_000802 See all 2 reported entries
MSCV MSCV_0003671
dbSNP ID rs41487950
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.
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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 0000003671 ?/? - . c.26T>C p.I9T - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000224206; RCV000854616;
Chromosome M:10084..10084
ClinVar Allele ID 237308
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.10084T>C
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:CA10581380
Gene symbol:Gene id. MT-ND3:4537
Allele origin germline
dbSNP ID 41487950
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