BRIP1 P210H
Gene Variant Detail

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Gene BRIP1
Variant P210H
Impact List missense
Protein Effect unknown
Gene Variant Descriptions BRIP1 P210H lies within the helicase ATP-binding domain of the Brip1 protein (UniProt.org). P210H has not been characterized and therefore, its effect on Brip1 protein function is unknown (PubMed, Feb 2026).
Associated Drug Resistance
Category Variants Paths

BRIP1 mutant BRIP1 P210H

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Transcript NM_032043.3
gDNA chr17:g.61808756G>T
cDNA c.629C>A
Protein p.P210H
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011525336.2 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525333.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436893.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436904.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436894.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
NM_032043.2 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525335.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525332.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525334.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
NM_032043.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436900.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525332.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525339.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525337.2 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525340.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525333.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525335.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525339.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436892.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525336.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436896.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436901.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436902.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436895.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525341.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436903.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436891.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436899.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_047436897.1 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525334.2 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525341.4 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38
XM_011525340.3 chr17:g.61808756G>T c.629C>A p.P210H RefSeq GRCh38/hg38

Filtering

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  • 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
BRIP1 mutant ovarian cancer not applicable N/A Guideline Risk Factor Germline BRIP1 mutations are associated with increased risk of developing ovarian cancer (NCCN.org). detail...