BRIP1 E501*
Gene Variant Detail

Request Content

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@genomenon.com

Gene BRIP1
Variant E501*
Impact List nonsense
Protein Effect loss of function - predicted
Gene Variant Descriptions BRIP1 E501* results in a premature truncation of the Brip1 protein at amino acid 501 of 1249 (UniProt.org). E501* has not been characterized, however, due to the effects of other truncation mutations downstream of E501 (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 E501*

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_032043.3
gDNA chr17:g.61784397C>A
cDNA c.1501G>T
Protein p.E501*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_047436899.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525334.2 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525336 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525340.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525339.4 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525339 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436894.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436896.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525339.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525334.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525335 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525335.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525336.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525336.2 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436891.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525332 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525332.4 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525341 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525333.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
NM_032043.2 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436895.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525341.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525341.4 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525332.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525340 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436893.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436904.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436900.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436897.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
NM_032043.3 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436902.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525333 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525337 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436903.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525333.4 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436901.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_047436892.1 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
NM_032043 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525334 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525337.2 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525335.4 chr17:g.61784397C>A c.1501G>T p.E501* RefSeq GRCh38/hg38
XM_011525340.4 chr17:g.61784397C>A c.1501G>T p.E501* 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