Variant #0000008685 (NC_000017.11:g.7676154G>C, TP53(NM_000546.5):c.215C>G)

Individual ID 00001533
Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.7676154G>C
Reference -
DB-ID TP53_000001 See all 49 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Dolores Mansilla-Instituto Roffo
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Zygosity     

Co_ocurrence     

Review status     
TP53 NM_000546.5 -/- 4 c.215C>G r.(?) p.(Pro72Arg) Homo no -



Screenings


AscendingScreening ID     

Template     

Technique     

Lab     

Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001805 DNA SEQ-NG CEMIC - 3-oct-2019 Multigenetic panel ATM, BRCA1, BRCA2, CHEK2, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, TP53 29 Dolores Mansilla-Instituto Roffo