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 ATR
Variant M211I
Impact List missense
Protein Effect unknown
Gene Variant Descriptions ATR M211I does not lie within any known functional domains of the Atr protein (UniProt.org). M211I has been identified in sequencing studies (PMID: 31173267), but has not been biochemically characterized and therefore, its effect on Atr protein function is unknown (PubMed, Aug 2024).
Associated Drug Resistance
Category Variants Paths

ATR mutant ATR M211I

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_001184.4
gDNA chr3:g.142562769C>G
cDNA c.633G>C
Protein p.M211I
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_001354579.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512925.2 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512925.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512924.2 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_047448360.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_047448362.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_047448364.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512924.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
NM_001184.3 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_017006643 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
NM_001184 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512924 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
NM_001184.4 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512926 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_047448361.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_047448363.1 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
NM_001354579.2 chr3:g.142562769C>G c.633G>C p.M211I RefSeq GRCh38/hg38
XM_011512925 chr3:g.142562769C>G c.633G>C p.M211I 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