View genomic variant #0000001440

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.9101T>C
Published as -
GERP 3.950
Segregation -
DB-ID chrM_000057 See all 2 reported entries
MSCV MSCV_0001440
dbSNP ID rs199476134
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 20301353;7726182
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-ATP6 00001337 MT-ATP6-201 0000001440 +/+ - . c.575T>C p.I192T - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010277; RCV000854439;
Chromosome M:9101..9101
ClinVar Allele ID 24682
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|Human Phenotype Ontology:HP:0001086, Human Phenotype Ontology:HP:0001112, MONDO:MONDO:0010788, MedGen:C0917796, OMIM:535000, Orphanet:104
ClinVar preferred disease name Leigh syndrome|Leber optic atrophy
HGVS variant names NC 012920.1:m.9101T>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:CA340927|OMIM:516060.0003
Gene symbol:Gene id. MT-ATP6:4508
Allele origin
dbSNP ID 199476134
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000854440;
Chromosome M:9101..9101
ClinVar Allele ID 681628
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.9101T>G
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Gene symbol:Gene id. MT-ATP6:4508
Allele origin germline
dbSNP ID 199476134
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-ATP6LHONT9101CI-T+-ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None