ERBB4 R306S
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 ERBB4
Variant R306S
Impact List missense
Protein Effect gain of function - predicted
Gene Variant Descriptions ERBB4 R306S lies within the extracellular domain of the Erbb4 protein (UniProt.org). R306S results in increased basal Erbb4 phosphorylation (PMID: 26050618), and therefore, is predicted to lead to a gain of Erbb4 protein function.
Associated Drug Resistance
Category Variants Paths

ERBB4 mutant ERBB4 act mut ERBB4 R306S

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_005235.3
gDNA chr2:g.211713616G>T
cDNA c.916C>A
Protein p.R306S
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_005246377 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_005246377.4 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_006712364.4 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_005235.2 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_001042599.1 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_006712364 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_005235 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_001042599 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_006712364.3 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_005246376 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_001042599.1 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
NM_005235.3 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_005246376.3 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_005246376.4 chr2:g.211713616G>T c.916C>A p.R306S RefSeq GRCh38/hg38
XM_005246377.3 chr2:g.211713616G>T c.916C>A p.R306S 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.

Clinical Trial Phase Therapies Title Recruitment Status Covered Countries Other Countries