BRIP1 T997fs
Gene Variant Detail

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Gene BRIP1
Variant T997fs
Impact List frameshift
Protein Effect loss of function - predicted
Gene Variant Descriptions BRIP1 T997fs results in a change in the amino acid sequence of the Brip1 protein beginning at aa 997 of 1249, likely resulting in premature truncation of the functional protein (UniProt.org). T997fs has not been characterized, however, due to the effects of other truncation mutations downstream of T997 (PMID: 18628483), is predicted to lead to a loss of Brip1 protein function.
Associated Drug Resistance
Category Variants Paths

BRIP1 mutant BRIP1 inact mut BRIP1 T997fs

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Transcript NM_032043.3
gDNA chr17:g.(61684057_61684058)
cDNA c.(2989_2988)
Protein p.T997fs
Source Database RefSeq
Genome Build 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.