View genomic variant #0000001507

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.14849T>C
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000044 See all 3 reported entries
MSCV MSCV_0001507
dbSNP ID rs207460004
Frequency -
Sources ; clinVar; Mitomap; Ensembl;
Reference 11891837
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 0000001507 +/+ - . c.103T>C p.S35P - - - -
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ClinVar @ MSeqDR

RCVaccession RCV000010323; RCV000855170; RCV002260587;
Chromosome M:14849..14849
ClinVar Allele ID 24724
Disease database name and identifier MONDO:MONDO:0044970, MeSH:D028361, MedGen:C0751651, Orphanet:68380|MedGen:C4016599|MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506
ClinVar preferred disease name Mitochondrial disease|Exercise intolerance, cardiomyopathy, and septooptic dysplasia|Leigh syndrome
HGVS variant names NC 012920.1:m.14849T>C
ClinVar review status reviewed by expert panel
Clinical Significance Uncertain significance
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA120623|Genetic Testing Registry (GTR):GTR000591967|Genetic Testing Registry (GTR):GTR000591975|Genetic Testing Registry (GTR):GTR000591976|OMIM:516020.0012
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207460004
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-CYBSepto-Optic DysplasiaT14849CS-P-+ReportedCoding_and_Control_Region

Ensembl Variant Phenotype Information:

None