View genomic variant #0000004157

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.15607A>G
Published as -
GERP 3.940
Segregation -
DB-ID chrM_000523 See all 3 reported entries
MSCV MSCV_0004157
dbSNP ID rs28357372
Frequency -
Sources ;
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.
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 0000004157 ?/? - . c.861A>G p.K287K - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000133457;
Chromosome M:15607..15607
ClinVar Allele ID 153649
Disease database name and identifier Human Phenotype Ontology:HP:0100615, MONDO:MONDO:0021068, MeSH:D010051, MedGen:C0919267, OMIM:167000
ClinVar preferred disease name Neoplasm of ovary
HGVS variant names NC 012920.1:m.15607A>G
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:CA345760
Gene symbol:Gene id. MT-CYB:4519
Allele origin unknown
dbSNP ID 193302996
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