View genomic variant #0000001509

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.15197T>C
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000046 See all 2 reported entries
MSCV MSCV_0001509
dbSNP ID rs207460001
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 11464242
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-CYB 00001350 MT-CYB-201 0000001509 +/+ - . c.451T>C p.S151P - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010320;
Chromosome M:15197..15197
ClinVar Allele ID 24721
Disease database name and identifier Human Phenotype Ontology:HP:0003546, MedGen:C0424551
ClinVar preferred disease name Exercise intolerance
HGVS variant names NC 012920.1:m.15197T>C
ClinVar review status no assertion criteria provided
Clinical Significance Pathogenic
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120620|OMIM:516020.0009
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207460001
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBEXITT15197CS-P-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None