View genomic variant #0000001514

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.15572T>C
Published as -
GERP 4.290
Segregation -
DB-ID chrM_000169 See all 2 reported entries
MSCV MSCV_0001514
dbSNP ID rs207459996
Frequency -
Sources ; clinVar; Ensembl;
Reference 9806551
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 0000001514 +/+ - . c.826T>C p.F276L - - - -
Legend  


ClinVar @ MSeqDR

RCVaccession RCV000010315; RCV002247304;
Chromosome M:15572..15572
ClinVar Allele ID 24716
Disease database name and identifier MedGen:CN169374|MONDO:MONDO:0023113, MedGen:CN280943
ClinVar preferred disease name not specified|Familial colorectal cancer
HGVS variant names NC 012920.1:m.15572T>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:CA250588|OMIM:516020.0004
Gene symbol:Gene id. MT-CYB:4519
Allele origin germline
dbSNP ID 207459996
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