Gene Variant Detail

Contact

Missing content? – Request curation!

Request curation for specific Genes, Variants, or PubMed publications.

Have questions, comments, or suggestions? - Let us know!

Email us at : ckbsupport@jax.org

Gene TP53
Variant P152fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 P152fs results in a change in the amino acid sequence of the Tp53 protein beginning at aa 152 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). P152fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of P152 (PMID: 31081129, PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon5 TP53 P152fs

TP53 mutant TP53 inact mut TP53 P152fs

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Transcript NM_000546.6
gDNA chr17:g.(7675158_7675159)
cDNA c.(454_453)
Protein p.P152fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001276696 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_000546 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276760.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407271.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407270.1 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407265.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126118.2 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126112 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276760 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276761.3 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126114 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276696.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407269.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276695 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276761.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126118 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407263.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276695.3 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276760.3 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407267.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276695.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276761 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001276696.3 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126118.1 chr17:g.(7674960_7674961) c.(454_453) p.P152fs RefSeq GRCh38/hg38
NM_001126113 chr17:g.(7675158_7675159) c.(454_453) p.P152fs RefSeq GRCh38/hg38

Filtering

  • Case insensitive filtering will display rows if any text in any cell matches the filter term
  • Use simple literal full or partial string matches
  • Separate multiple filter terms with a space. Any order may be used (i. e. a b c and c b a are equivalent )
  • Filtering will only apply to rows that are already loaded on the page. Filtering has no impact on query parameters.
  • Use quotes to match on a longer phrase with spaces (i.e. "mtor c1483f")

Sorting

  • Generally, the default sort order for tables is set to be first column ascending; however, specific tables may set a different default sort order.
  • Click on any column header arrows to sort by that column
  • Hold down the Shift key and click multiple columns to sort by more than one column. Be sure to set ascending or descending order for a given column before moving on to the next column.

Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References