PDGFRB E134G
Gene Variant Detail

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Gene PDGFRB
Variant E134G
Impact List missense
Protein Effect unknown
Gene Variant Descriptions PDGFRB E134G lies within Ig-like C2-type domain 2 of the Pdgfrb protein (UniProt.org). E134G has been identified in sequencing studies (PMID: 22810696), but has not been biochemically characterized and therefore, its effect on Pdgfrb protein function is unknown (PubMed, Mar 2026).
Associated Drug Resistance
Category Variants Paths

PDGFRB mutant PDGFRB E134G

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Transcript NM_002609.4
gDNA chr5:g.150134980T>C
cDNA c.401A>G
Protein p.E134G
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011537658 chr5:g.150134980T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_001355017.1 chr5:g.150133636T>C c.401A>G p.E134G RefSeq GRCh38/hg38
XM_005268464 chr5:g.150134788T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_002609 chr5:g.150134980T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_002609.3 chr5:g.150134980T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_001355016.1 chr5:g.150134788T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_001355017.2 chr5:g.150133636T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_001355016.2 chr5:g.150134788T>C c.401A>G p.E134G RefSeq GRCh38/hg38
NM_002609.4 chr5:g.150134980T>C c.401A>G p.E134G RefSeq GRCh38/hg38
XM_011537659 chr5:g.150134980T>C c.401A>G p.E134G 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

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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References