Gene Variant Detail

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 RET
Variant A756V
Impact List missense
Protein Effect loss of function - predicted
Gene Variant Descriptions RET A756V lies within the protein kinase domain of the Ret protein (UniProt.org). A756V results in reduced phosphorylation of Ret and Erk in cell culture (PMID: 26395553), and therefore, is predicted to lead to a loss of Ret protein function.
Associated Drug Resistance
Category Variants Paths

RET mutant RET inact mut RET A756V

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_020975.6
gDNA chr10:g.43116714C>T
cDNA c.2267C>T
Protein p.A756V
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_020975 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_001406760.1 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_020630 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_020975.5 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_020975.6 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_020630.5 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43116714C>T c.2267C>T p.A756V RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43116714C>T c.2267C>T p.A756V 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