All variants in the TP53 gene

Information The variants shown are described using the NM_000546.5 transcript reference sequence.

4 entries on 1 page. Showing entries 1 - 4.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
?/. 2 c.28G>A r.(?) p.(Val10Ile) - VUS g.7579885C>T g.7676567C>T - - TP53_010121 not in 7051 cases breast cancer PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs535274413 Germline - 1/11241 controls - 0 - Yukihide Momozawa
?/. - c.28G>A r.(?) p.(Val10Ile) - VUS g.7579885C>T g.7676567C>T - - TP53_010121 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs535274413 Germline - 2/12454 controls - 0 - Yukihide Momozawa
?/. - c.28G>A r.(?) p.(Val10Ile) - NA g.7579885C>T - chr17_7579885_C_T - TP53_010121 the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 2/60466 cases - 0 - BRIDGES consortium
?/. - c.28G>A r.(?) p.(Val10Ile) - NA g.7579885C>T - chr17_7579885_C_T - TP53_010121 the study was not designed to clinically classify individual variants but performed burden-type association analyses, grouping certain variant types PubMed: Dorling 2021, Journal: Dorling 2021 - - Germline - 1/53461 controls - 0 - BRIDGES consortium
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