View genomic variant #0000004651

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.5556G>C
Published as -
GERP 4.360
Segregation -
DB-ID chrM_000315
MSCV MSCV_0004651
dbSNP ID rs387906736
Frequency -
Sources ; clinVar; Mitomap; ensembl;
Reference 19809478
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-TW 00001326 MT-TW-201 0000004651 +/+ - . . . - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000022907;
Chromosome M:5556..5556
ClinVar Allele ID 38962
Disease database name and identifier MONDO:MONDO:0004675, MedGen:C0162666
ClinVar preferred disease name Mitochondrial encephalomyopathy
HGVS variant names NC 012920.1:m.5556G>A
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:CA128833|OMIM:590095.0006
Gene symbol:Gene id. MT-TW:4578
Allele origin germline
dbSNP ID 387906736
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

LocusDiseaseAlleleAmino_Acid_ChangeHomoplasmyHeteroplasmySTATUSNote
MT-TWCombined OXPHOS defectsG5556AtRNA Trp-+ReportedRNA
MT-TWMito encephalomyopathyG5556CtRNA Trp-+ReportedRNA

Ensembl Variant Phenotype Information:

None