View genomic variant #0000001508

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.14985G>A
Published as -
GERP 4.150
Segregation -
DB-ID chrM_000045 See all 3 reported entries
MSCV MSCV_0001508
dbSNP ID rs207459995
Frequency -
Sources ; clinVar; Ensembl;
Reference 9806551;13298683
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 0000001508 +/+ - . c.239G>A p.R80H - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010314; RCV000855200;
Chromosome M:14985..14985
ClinVar Allele ID 24715
Disease database name and identifier MONDO:MONDO:0009723, MedGen:C0023264, OMIM:256000, Orphanet:506|MONDO:MONDO:0023113, MedGen:CN280943
ClinVar preferred disease name Leigh syndrome|Familial colorectal cancer
HGVS variant names NC 012920.1:m.14985G>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:CA250587|OMIM:516020.0003
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207459995
Variant Flags
:

ClinVar @ MSeqDR as full content XML tree

MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None