BRIP1 L134V
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 L134V
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRIP1 L134V lies within the helicase ATP-binding domain of the Brip1 protein (UniProt.org). L134V has not been characterized in the scientific literature and therefore, its effect on Brip1 protein function is unknown (PubMed, Jun 2026).
Associated Drug Resistance
Category Variants Paths

BRIP1 mutant BRIP1 L134V

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.61849236G>C
cDNA c.400C>G
Protein p.L134V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011525333 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525335.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525332.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436903.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436902.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436899.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
NM_032043 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525333.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525334 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436901.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525339 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
NM_032043.2 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436895.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525340.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525341.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525337.2 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525340 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525341.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525336 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436891.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436892.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525336.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525335.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525341 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525340.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525332.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525339.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525339.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436896.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436894.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525334.2 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525333.4 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436900.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525336.2 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525335 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525334.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436893.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525332 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436904.1 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_011525337 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
NM_032043.3 chr17:g.61849236G>C c.400C>G p.L134V RefSeq GRCh38/hg38
XM_047436897.1 chr17:g.61849236G>C c.400C>G p.L134V 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