CDKN2A A76T
Gene Variant Detail

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Gene CDKN2A
Variant A76T
Impact List missense
Protein Effect unknown
Gene Variant Descriptions CDKN2A A76T does not lie within any known functional domains of the Cdkn2a protein (UniProt.org). A76T has been identified in sequencing studies (PMID: 31004019, PMID: 26164066, PMID: 34915860), but has not been biochemically characterized and therefore, its effect on Cdkn2a protein function is unknown (PubMed, Jun 2025).
Associated Drug Resistance
Category Variants Paths

CDKN2A mutant CDKN2A A76T

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Transcript NM_000077.5
gDNA chr9:g.21971133C>T
cDNA c.226G>A
Protein p.A76T
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_011517675.2 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517676 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_047422596.1 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_058195 chr9:g.21971176C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_058195.3 chr9:g.21971176C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517679.1 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_001195132.2 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_001195132 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_000077.4 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_047422598.1 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517676.3 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517675.3 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517679 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_047422597.1 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_000077.5 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_000077 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517675 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_005251343.1 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_005251343 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_001195132.1 chr9:g.21971133C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_001363763.2 chr9:g.21970980C>T c.226G>A p.A76T RefSeq GRCh38/hg38
NM_058195.4 chr9:g.21971176C>T c.226G>A p.A76T RefSeq GRCh38/hg38
XM_011517676.2 chr9:g.21971133C>T c.226G>A p.A76T 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.
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Molecular Profile Indication/Tumor Type Response Type Therapy Name Approval Status Evidence Type Efficacy Evidence References