View genomic variant #0000001361

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.4269A>G
Published as -
GERP 4.530
Segregation -
DB-ID chrM_000006 See all 2 reported entries
MSCV MSCV_0001361
dbSNP ID rs121434466
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 1632786
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 0000001361 +/+ - . . . - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010225; RCV002247291;
Chromosome M:4269..4269
ClinVar Allele ID 24641
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:C4016613
ClinVar preferred disease name Mitochondrial disease|Cardiomyopathy, fatal
HGVS variant names NC 012920.1:m.4269A>G
ClinVar review status criteria provided, single submitter
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120570|OMIM:590045.0002
Gene symbol:Gene id. MT-TI:4565
Allele origin germline
dbSNP ID 121434466
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TIFICPA4269GtRNA Ile-+ReportedRNA

Ensembl Variant Phenotype Information:

None