FGFR3 C228R
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 FGFR3
Variant C228R
Impact List missense
Protein Effect gain of function - predicted
Gene Variant Descriptions FGFR3 C228R lies within Ig-like C2-type domain 2 of the Fgfr3 protein (UniProt.org). C228R results in the stabilization of Fgfr3 dimers in culture (PMID: 27596331), and therefore, is predicted to lead to a gain of Fgfr3 protein function.
Associated Drug Resistance
Category Variants Paths

FGFR3 mutant FGFR3 act mut FGFR3 C228R

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_000142.5
gDNA chr4:g.1801686T>C
cDNA c.682T>C
Protein p.C228R
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_047449820.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513422.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001354810.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713869 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513420.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713871.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001354809.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713871 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713869.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001163213.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713868 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713868.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001354809.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713868.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_000142 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713871.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713873.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513422.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713869.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513422 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001354810.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713873.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_047449823.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513420 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_022965.3 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713870 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713870.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_022965 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_047449824.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713873 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_022965.4 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_011513420.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713872 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_047449821.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001163213 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_000142.4 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_006713870.2 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
XM_047449822.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_001163213.1 chr4:g.1801686T>C c.682T>C p.C228R RefSeq GRCh38/hg38
NM_000142.5 chr4:g.1801686T>C c.682T>C p.C228R 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