Gene Variant Detail

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Gene RET
Variant A883X
Impact List missense
Protein Effect unknown
Gene Variant Descriptions RET A883X indicates any Ret missense mutation that results in replacement of the alanine (A) at amino acid 883 by a different amino acid.
Associated Drug Resistance
Category Variants Paths

RET mutant RET A883X

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Transcript NM_020975.6
gDNA chr10:g.43120120_43120122
cDNA c.2647_2649
Protein p.A883
Source Database RefSeq
Genome Build GRCh38/hg38
Transcript gDNA cDNA Protein Source Database Genome Build
NM_020630.5 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_001406744.1 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_001406760.1 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_020975 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_001406759.1 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_020975.5 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_020630.7 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_001406743.1 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_020630 chr10:g.43120120_43120122 c.2647_2649 p.A883 RefSeq GRCh38/hg38
NM_020975.6 chr10:g.43120120_43120122 c.2647_2649 p.A883 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
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Molecular Profile Protein Effect Treatment Approaches
RET A883X unknown