View genomic variant #0000001513

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.15498G>A
Published as -
GERP 3.130
Segregation -
DB-ID chrM_000050 See all 2 reported entries
MSCV MSCV_0001513
dbSNP ID rs207460003
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 10960495
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-CYB 00001350 MT-CYB-201 0000001513 +/+ - . c.752G>A p.G251D - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010322; RCV000855308;
Chromosome M:15498..15498
ClinVar Allele ID 24723
Disease database name and identifier Human Phenotype Ontology:HP:0005152, MONDO:MONDO:0010771, MedGen:C1708371, OMIM:500000, Orphanet:137675|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Histiocytoid cardiomyopathy|Leigh syndrome
HGVS variant names NC 012920.1:m.15498G>A
ClinVar review status criteria provided, single submitter
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120622|OMIM:516020.0011
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207460003
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBEXIT15498del24GDPDNYTL-del-+ReportedCoding_and_Control_Region
MT-CYBHiCM / WPW, DEAFG15498AG-D-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None