View genomic variant #0000004078

Chromosome M
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Type subst
DNA change (genomic) (Relative to hg19 / GRCh37) m.14783T>C
Published as -
GERP 1.110
Segregation -
DB-ID chrM_000451 See all 3 reported entries
MSCV MSCV_0004078
dbSNP ID rs28357680
Frequency -
Sources ; Ensembl;
Reference -
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 0000004078 +?/+? - . c.37T>C p.L13L - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000128803;
Chromosome M:14783..14783
ClinVar Allele ID 150280
Disease database name and identifier MONDO:MONDO:0016419, MedGen:C0346153, OMIM:114480, Orphanet:227535
ClinVar preferred disease name Familial cancer of breast
HGVS variant names NC 012920.1:m.14783T>C
ClinVar review status criteria provided, single submitter
Clinical Significance Benign
Variant type single nucleotide variant
Sequence Ontology for variant type SO:0001483
Variant clinical sources reported ClinGen:CA345704
Gene symbol:Gene id. MT-CYB:4519
Allele origin unknown
dbSNP ID 193302982
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