ClinVar

NM_000546.6(TP53):c.455C>T (p.Pro152Leu)

Gene:

TP53:tumor protein p53 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

17p13.1

Genomic location:

• Chr17: 7675157 (on Assembly GRCh38)
• Chr17: 7578475 (on Assembly GRCh37)

Preferred name:

NM_000546.6(TP53):c.455C>T (p.Pro152Leu)

HGVS:

• NC_000017.11:g.7675157G>A
• NG_017013.2:g.17394C>T
• NM_000546.6:c.455C>TMANE SELECT
• NM_001126112.3:c.455C>T
• NM_001126113.3:c.455C>T
• NM_001126114.3:c.455C>T
• NM_001126115.2:c.59C>T
• NM_001126116.2:c.59C>T
• NM_001126117.2:c.59C>T
• NM_001126118.2:c.338C>T
• NM_001276695.3:c.338C>T
• NM_001276696.3:c.338C>T
• NM_001276697.3:c.-23C>T
• NM_001276698.3:c.-23C>T
• NM_001276699.3:c.-23C>T
• NM_001276760.3:c.338C>T
• NM_001276761.3:c.338C>T
• NP_000537.3:p.Pro152Leu
• NP_000537.3:p.Pro152Leu
• NP_001119584.1:p.Pro152Leu
• NP_001119585.1:p.Pro152Leu
• NP_001119586.1:p.Pro152Leu
• NP_001119587.1:p.Pro20Leu
• NP_001119588.1:p.Pro20Leu
• NP_001119589.1:p.Pro20Leu
• NP_001119590.1:p.Pro113Leu
• NP_001263624.1:p.Pro113Leu
• NP_001263625.1:p.Pro113Leu
• NP_001263689.1:p.Pro113Leu
• NP_001263690.1:p.Pro113Leu
• LRG_321t1:c.455C>T
• LRG_321:g.17394C>T
• LRG_321p1:p.Pro152Leu
• NC_000017.10:g.7578475G>A
• NM_000546.4:c.455C>T
• NM_000546.5(TP53):c.455C>T
• NM_000546.5:c.455C>T
• P04637:p.Pro152Leu
• p.P152L

This HGVS expression did not pass validation

Protein change:

P113L

Links:

UniProtKB: P04637#VAR_005897; dbSNP: rs587782705

NCBI 1000 Genomes Browser:

rs587782705

Molecular consequence:

• NM_001276697.3:c.-23C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276698.3:c.-23C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_001276699.3:c.-23C>T - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
• NM_000546.6:c.455C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126112.3:c.455C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126113.3:c.455C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126114.3:c.455C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126115.2:c.59C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126116.2:c.59C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126117.2:c.59C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001126118.2:c.338C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001276695.3:c.338C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001276696.3:c.338C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001276760.3:c.338C>T - missense variant - [Sequence Ontology: SO:0001583]
• NM_001276761.3:c.338C>T - missense variant - [Sequence Ontology: SO:0001583]