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 V274fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions TP53 V274fs results in a change in the amino acid sequence of the Tp53 protein beginning at aa 274 of 393, likely resulting in premature truncation of the functional protein (UniProt.org). V274fs has not been biochemically characterized however, due to the effects of truncation mutations downstream of V274 (PMID: 31081129PMID: 34045312), is predicted to lead to a loss of Tp53 protein function.
Associated Drug Resistance
Category Variants Paths

TP53 mutant TP53 exon8 TP53 V274fs

TP53 mutant TP53 inact mut TP53 V274fs

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.(7673800_7673801)
cDNA c.(820_819)
Protein p.V274fs
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001407270.1 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001407262.1 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126113.2 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_000546.5 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001407268.1 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126114.2 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126114.3 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001407266.1 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001407264.1 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_000546.6 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126112.2 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126113.3 chr17:g.(7673800_7673801) c.(820_819) p.V274fs RefSeq GRCh38/hg38
NM_001126112.3 chr17:g.(7673800_7673801) c.(820_819) p.V274fs 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