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.27C>T r.(?) p.(=) - benign g.7579886G>A g.7676568G>A - - TP53_010122 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs757282628 Germline - 1/7051 cases breast cancer - 0 - Yukihide Momozawa
-/. 2 c.27C>T r.(?) p.(=) - benign g.7579886G>A g.7676568G>A - - TP53_010122 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs757282628 Germline - 3/11241 controls - 0 - Yukihide Momozawa
-/. - c.27C>T r.(?) p.(=) - benign g.7579886G>A g.7676568G>A - - TP53_010122 - PubMed: Momozawa 2018, Journal: Momozawa 2018 - rs757282628 Germline - 3/12454 controls - 0 - Yukihide Momozawa
-?/. - c.27C>T r.(?) p.(Ser9=) - likely benign g.7579886G>A g.7676568G>A TP53(NM_000546.5):c.27C>T (p.S9=) - TP53_010122 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_NKI
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