Variant #0000402982 (NC_000017.10:g.7579579C>T, TP53(NM_000546.5):c.108G>A)

Individual ID 00178618
Chromosome 17
Allele Parent #1
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7579579C>T
DNA change (hg38) g.7676261C>T
Published as -
ISCN -
DB-ID TP53_010050 See all 11 reported entries
Variant remarks -
Reference PubMed: Momozawa 2018, Journal: Momozawa 2018
ClinVar ID -
dbSNP ID rs1800370
Origin Germline
Segregation -
Frequency 36/7051 cases breast cancer
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01324 View details
Owner Yukihide Momozawa
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TP53 NM_000546.5 -/. 4 c.108G>A r.(?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000179521 DNA SEQ - - TP53 1 Yukihide Momozawa