SRC Y530*
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 SRC
Variant Y530*
Impact List nonsense
Protein Effect unknown
Gene Variant Descriptions SRC Y530* results in a premature truncation of the Src protein at amino acid 530 of 536 (UniProt.org). Y530* has not been characterized in the scientific literature and therefore, its effect on Src protein function is unknown (PubMed, Oct 2025).
Associated Drug Resistance
Category Variants Paths

SRC mutant SRC Y530*

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_198291.3
gDNA chr20:g.37403358C>A
cDNA c.1590C>A
Protein p.Y530*
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_005417 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440411.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
NM_198291.3 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
NM_005417.5 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440401.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440403.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_011529013.2 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_011529013 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
NM_198291 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440405.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440413.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440404.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
NM_005417.4 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440412.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
NM_198291.2 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440402.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440406.1 chr20:g.37403358C>A c.1590C>A p.Y530* RefSeq GRCh38/hg38
XM_047440410.1 chr20:g.37403358C>A c.1590C>A p.Y530* 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