View genomic variant #0000001360

Chromosome M
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Probably does not affect function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.4216T>C
Published as -
GERP -6.780
Segregation -
DB-ID chrM_000005 See all 4 reported entries
MSCV MSCV_0001360
dbSNP ID rs1599988
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 7635294;1732158;1900003;20301353
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 0000001360 -?/-? - . c.910T>C p.T304H - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010373; RCV000709875; RCV000853749;
Chromosome M:4216..4216
ClinVar Allele ID 24763
Disease database name and identifier MedGen:CN517202|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 not provided|Leber optic atrophy|Leigh syndrome
HGVS variant names NC 012920.1:m.4216T>C
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:CA340943|OMIM:516000.0003
Gene symbol:Gene id. MT-ND1:4535
Allele origin germline
dbSNP ID 1599988
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ND1LHON/Insulin ResistanceT4216CY-H+-P.M. - haplogroup J/T markerCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None