View genomic variant #0000004548

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.4312C>T
Published as -
GERP 2.520
Segregation -
DB-ID chrM_001304
MSCV MSCV_0004548
dbSNP ID rs200931747
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-TI 00001322 MT-TI-201 0000004548 ?/? - . . . - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000850723;
Chromosome M:4312..4312
ClinVar Allele ID 677714
Disease database name and identifier MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 012920.1:m.4312C>T
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-TI:4565
Allele origin germline
dbSNP ID 193303033
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

ClinVar @ MSeqDR

RCVaccession RCV000850727;
Chromosome M:4313..4313
ClinVar Allele ID 677716
Disease database name and identifier MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 012920.1:m.4314del
ClinVar review status criteria provided, single submitter
Clinical Significance Likely benign
Variant type Deletion
Sequence Ontology for variant type SO:0000159
Gene symbol:Gene id. MT-TI:4565
Allele origin germline
dbSNP ID 1603219400
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