BRIP1 I507M
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@genomenon.com

Gene BRIP1
Variant I507M
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRIP1 I507M does not lie within any known functional domains of the Brip1 protein (UniProt.org). I507M has not been characterized in the scientific literature and therefore, its effect on Brip1 protein function is unknown (PubMed, Feb 2026).
Associated Drug Resistance
Category Variants Paths

BRIP1 mutant BRIP1 I507M

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.61784377A>C
cDNA c.1521T>G
Protein p.I507M
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_032043.2 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436891.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525334.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
NM_032043 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436897.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525332 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436903.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436892.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525337 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525337.2 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525339 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525335.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525341 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525332.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525336.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525333.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436900.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436899.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436901.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525335.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525333 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525334 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525336 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436896.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436895.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525335 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525340 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525334.2 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
NM_032043.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525333.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436893.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525341.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436894.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525340.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525340.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525336.2 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525339.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525341.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525332.3 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436902.1 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_011525339.4 chr17:g.61784377A>C c.1521T>G p.I507M RefSeq GRCh38/hg38
XM_047436904.1 chr17:g.61784377A>C c.1521T>G p.I507M 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