ERBB4 I166N
Gene Variant Detail

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Gene ERBB4
Variant I166N
Impact List missense
Protein Effect unknown
Gene Variant Descriptions ERBB4 I166N lies within the extracellular domain of the Erbb4 protein (UniProt.org). I166N has been identified in sequencing studies (PMID: 30115035, PMID: 22810696, PMID: 34987087), but has not been biochemically characterized and therefore, its effect on Erbb4 protein function is unknown (PubMed, May 2026).
Associated Drug Resistance
Category Variants Paths

ERBB4 mutant ERBB4 I166N

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Transcript NM_005235.3
gDNA chr2:g.211788084A>T
cDNA c.497T>A
Protein p.I166N
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_017003578.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003581 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_005235 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_001042599.1 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_005235.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246377 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003582.2 chr2:g.211712056A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003580 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003579.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003577.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003582.1 chr2:g.211712056A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003577 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003579.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003578 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_001042599.1 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003578.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003580.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246377.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003579 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246377.4 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_001042599 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003581.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003577.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_006712364 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
NM_005235.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_006712364.4 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246376.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003580.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246376 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003582 chr2:g.211712056A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_017003581.2 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_006712364.3 chr2:g.211788084A>T c.497T>A p.I166N RefSeq GRCh38/hg38
XM_005246376.4 chr2:g.211788084A>T c.497T>A p.I166N 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
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Molecular Profile Protein Effect Treatment Approaches
ERBB4 I166N unknown