Annotation Detail

Information
Associated Genes
TP53
Associated Variants
TP53 p.Pro72Arg (p.P72R) ( ENST00000359597.8, ENST00000413465.6, ENST00000604348.6, ENST00000269305.9, ENST00000455263.6, ENST00000420246.6, ENST00000445888.6, ENST00000576024.2, ENST00000610292.4, ENST00000610538.4, ENST00000619485.4, ENST00000620739.4, ENST00000622645.4, ENST00000714356.1, ENST00000714357.1, ENST00000714359.1, ENST00000714408.1, ENST00000714409.1 )
TP53 p.Pro72Arg (p.P72R) ( ENST00000269305.9, ENST00000359597.8, ENST00000413465.6, ENST00000420246.6, ENST00000445888.6, ENST00000455263.6, ENST00000576024.2, ENST00000604348.6, ENST00000610292.4, ENST00000610538.4, ENST00000619485.4, ENST00000620739.4, ENST00000622645.4, ENST00000714356.1, ENST00000714357.1, ENST00000714359.1, ENST00000714408.1, ENST00000714409.1 )
Associated Disease
CODON 72 POLYMORPHISM
Source Database
ClinVar
Description
NM_000546.6(TP53):c.215C>G (p.Pro72Arg) AND CODON 72 POLYMORPHISM
ClinVar Allele ID
27390
ClinVar RefSeq Alternation Syntax
NM_001126118.2:c.98C>G
ClinVar RefSeq Alternation Syntax
NM_001276761.3:c.98C>G
ClinVar RefSeq Alternation Syntax
NM_001126114.3:c.215C>G
ClinVar RefSeq Alternation Syntax
NM_001126112.3:c.215C>G
ClinVar RefSeq Alternation Syntax
NM_001276696.3:c.98C>G
ClinVar RefSeq Alternation Syntax
NM_001276760.3:c.98C>G
ClinVar RefSeq Alternation Syntax
NM_001126113.3:c.215C>G
ClinVar RefSeq Alternation Syntax
NM_000546.6:c.215C>G
ClinVar RefSeq Alternation Syntax
NM_001276695.3:c.98C>G
Clinical Significance Description
Benign
Clinical Significance Last Update
2009-10-01
Clinical Significance Review Status
no assertion criteria provided
URL
https://www.ncbi.nlm.nih.gov/clinvar/RCV000013144
ClinVar Disease
CODON 72 POLYMORPHISM
Observed Origin Sample
unknown
Pubmed
15355915
Pubmed
16964264
Pubmed
1999338
Pubmed
16258005
Pubmed
12567188
Pubmed
9607760
Pubmed
10802655
Pubmed
16199549
Pubmed
17535973
Pubmed
19521721
Pubmed
9891044
Pubmed
11403041
Pubmed
1975675
Pubmed
8242752
Drugs