View genomic variant #0000004535

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.4277T>C
Published as -
GERP -9.060
Segregation -
DB-ID chrM_000683 See all 2 reported entries
MSCV MSCV_0004535
dbSNP ID -
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.
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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 0000004535 +?/+? - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000223876; RCV000850715; RCV001009555;
Chromosome M:4277..4277
ClinVar Allele ID 236830
Disease database name and identifier MedGen:CN517202|MedGen:CN169374|MONDO:MONDO:0010789, MedGen:C0162671, OMIM:540000, Orphanet:550
ClinVar preferred disease name not provided|not specified|Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
HGVS variant names NC 012920.1:m.4277T>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:CA10581200
Gene symbol:Gene id. MT-TI:4565
Allele origin germline
dbSNP ID 876661358
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TIPoss. hypertension factorT4277CtRNA Ile+-ReportedRNA

Ensembl Variant Phenotype Information:

None