MST1R R396Q
Gene Variant Detail

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Gene MST1R
Variant R396Q
Impact List missense
Protein Effect unknown
Gene Variant Descriptions MST1R R396Q lies within the Sema domain of the Mst1r protein (UniProt.org). R396Q has been identified in sequencing studies (PMID: 29420467), but has not been biochemically characterized and therefore, its effect on Mst1r protein function is unknown (PubMed, Mar 2026).
Associated Drug Resistance
Category Variants Paths

MST1R mutant MST1R R396Q

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Transcript NM_002447.4
gDNA chr3:g.49902423C>T
cDNA c.1187G>A
Protein p.R396Q
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
XM_047448163.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_002447 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001318913 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448165.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448174.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533743.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533741 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001318913.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_005265170 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533741.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448173.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533740.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448180.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448178.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448171.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533741.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448162.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_002447.4 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001318913.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533744 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533744.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448170.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448172.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448179.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001244937 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448168.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001244937.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_005265170.5 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533739 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533742.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448164.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448167.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533743.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533740 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_005265170.4 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448176.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533740.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533739.2 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533739.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533744.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448169.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533742 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448166.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448175.1 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_001244937.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533742.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_011533743 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
NM_002447.3 chr3:g.49902423C>T c.1187G>A p.R396Q RefSeq GRCh38/hg38
XM_047448177.1 chr3:g.49902423C>T c.1187G>A p.R396Q 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