All variants in the TP53 gene

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

7 entries on 1 page. Showing entries 1 - 7.
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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.31G>C r.(?) p.(Glu11Gln) - benign g.7579882C>G g.7676564C>G - - TP53_010120 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs201382018 Germline - 95/7051 cases breast cancer - 0 - Yukihide Momozawa
-/. 2 c.31G>C r.(?) p.(Glu11Gln) - benign g.7579882C>G g.7676564C>G - - TP53_010120 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs201382018 Germline - 172/11214 controls - 0 - Yukihide Momozawa
-/. - c.31G>C r.(?) p.(Glu11Gln) - benign g.7579882C>G g.7676564C>G - - TP53_010120 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs201382018 Germline - 1/7051 cases breast cancer - 0 - Yukihide Momozawa
-/. - c.31G>C r.(?) p.(Glu11Gln) - benign g.7579882C>G g.7676564C>G - - TP53_010120 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs201382018 Germline - 1/53 cases - 0 - Yukihide Momozawa
-/. - c.31G>C r.(?) p.(Glu11Gln) - benign g.7579882C>G g.7676564C>G - - TP53_010120 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs201382018 Germline - 184/12451 controls - 0 - Yukihide Momozawa
?/. - c.31G>C r.(?) p.(Glu11Gln) - NA g.7579882C>G - chr17_7579882_C_G - TP53_010119 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 - 16/60466 cases - 0 - BRIDGES consortium
?/. - c.31G>C r.(?) p.(Glu11Gln) - NA g.7579882C>G - chr17_7579882_C_G - TP53_010119 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 - 9/53461 controls - 0 - BRIDGES consortium
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