Variant #0000008384 (NC_000017.11:g.7676154G>C, TP53(NM_000546.5):c.215C>G)

Individual ID 00001497
Chromosome 17
Allele Unknown
Affects function (as reported) Not classified
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 Silvina Sisterna-Hospital de Comunidad
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     

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DNA change (cDNA)     

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



Screenings


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Variants found     

Owner     
0000001766 DNA CNV;SEQ-NG IACA Panel (ATM, BARD1, BRCA1/2, BRP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53) 21-may-2020 Multigenetic panel - 47 Silvina Sisterna-Hospital de Comunidad