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  • FILTER
    Mutation Type
      Deletion
          Frameshift
          Inframe
      Insertion
          Frameshift
          Inframe
      Substitution
          Nonsense
          Missense
          Synonymous
      Complex
    Sample Source
      Cultured Sample
      Tumour Sample
    Somatic Status
     Confirmed Somatic
     Previously Reported
     Variant of unknown       origin
    Systematic Screen
     From Systematic       Screen
    Current Selection
  • Genes Chosen
    RET
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Distribution of somatic mutations in RET

 

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cDNA Amino Acid

There are 4 additional mutations not displayed in the above image, as they are without positional information.

here
Details For Mutation Type Chart
  Mutation TypeNumberPercentageMutation Data
 Deletion Frameshift00.0 %

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 Deletion Inframe113.1 %

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 Insertion Frameshift00.0 %

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 Insertion Inframe00.0 %

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 Substitution Nonsense00.0 %

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 Substitution Missense30888.0 %

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 Substitution Synonymous61.7 %

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 Complex216.0 %

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 Other41.1 %

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 Total350100%More Details
here
Details for Sample Source Chart
  Sample SourceNumberPercentageSource Data
 Cultured Sample72.0 %

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 Tumour Sample32593.1 %

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 NS174.9 %

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 Total349100%More Details
Substitutions
Position Mutation(n)
145 p.V145G(1)
163 p.R163Q(1)
348 p.R348R(1)
360 p.R360W(1)
373 p.A373A(1)
591 p.V591I(1)
593 p.G593E(1)
609 p.C609Y(1)
618 p.C618R(1) p.C618Y(1)
620 p.C620R(1) p.C620S(1)
630 p.C630G(1) p.C630R(3) p.C630R(1)
631 p.D631G(1)
634 p.C634A(1) p.C634C(1) p.C634R(8) p.C634R(5) p.C634T(1) p.C634W(4) p.C634W(3) p.C634Y(4) p.C634Y(1)
664 p.A664D(2)
748 p.G748C(1)
766 p.P766S(1)
768 p.E768D(4)
778 p.V778V(1)
792 p.G792G(1)
876 p.A876V(1)
883 p.A883F(4) p.A883F(1) p.A883F(1) p.A883P(1) p.A883S(1)
884 p.E884K(1)
901 p.E901K(1)
908 p.R908K(1)
911 p.G911D(1)
918 p.M918T(232) p.M918T(13)
919 p.A919V(1)
921 p.E921K(1)
922 p.S922P(1)
925 p.D925H(1)
930 p.T930M(1)
974 p.D974D(1)
1112 p.F1112Y(1)
 
Insertions
Position Mutation(n)
No Insertions in Current Selection
 
Deletions
Position Mutation(n)
592 p.G592_G607del(1)
612 p.F612_C620del(1)
632 p.E632_L633del(6) p.E632_L633del(1)
898 p.D898_E901del(1) p.D898_E901del(1)
 
Complex
Position Mutation(n)
627 p.D627_L633>E(1)
629 p.L629_D631>H(2)
631 p.D631_L633>E(1)
632 p.E632_A640>VRP(1) p.E632_C634>L(1) p.E632_L633>V(1) p.E632_T636>SS(14)
 
Fusion Mutations
Mutation(n)
No Fusion Mutations in Current Selection
 
Other Mutations
Position Mutation(n)
p.?(3) p.?(1)
 
  
 Details for RET 
Primary Tissue Unique Mutated Samples % Mutated Total Unique Samples Mutation Data 
NS00%2

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adrenal gland196%324

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autonomic ganglia00%183

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biliary tract00%6

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bone00%32

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breast00%100

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central nervous system11%177

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cervix00%13

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endometrium00%10

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eye00%1

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gastrointestinal tract (site indeterminate)00%11

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haematopoietic and lymphoid tissue00%154

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kidney00%45

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large intestine54%142

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liver00%10

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lung31%232

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oesophagus00%23

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ovary12%47

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pancreas00%57

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parathyroid00%182

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pituitary00%180

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placenta00%2

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pleura00%6

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prostate00%5

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salivary gland00%10

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skin00%57

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small intestine00%1

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soft tissue00%23

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stomach00%41

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testis00%17

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thyroid31934%944

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upper aerodigestive tract00%39

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urinary tract16%18

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vulva00%3

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Totals 34911% 3097

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Last Modified Mon Sep 18 17:13:20 2006

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