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. Author manuscript; available in PMC: 2019 Jan 1.
Published in final edited form as: Environ Mol Mutagen. 2017 Nov 8;59(1):18–29. doi: 10.1002/em.22154

Table 2.

Mutation sequencing data from 38 individual CD90-deficient clones derived from the culture of L5178Y/Tk+/− cells treated with EMS

Litron ID Primary X-
chromosome
mutation
Primary
mutation
frequency
Amino acid
change
Litron ID Primary X-
chromosome
mutation
Primary
mutation
frequency
Amino acid
change
a-c3 164423363 G>A 0.99 Splice site b2–b4 164428596 G>A 0.99 Gly>Glu
a-c5 164423346 G>A 0.99 Arg>Lys b2-c4 164423087 C>T 0.99 Gln>Stop
a-d2 164428832 G>A 0.99 Gly>Arg b2-c6 164428539 G>A 0.99 Splice site
a-d2 164428832 G>A 0.99 Gly>Arg b2-d1 164428833 G>A 0.99 Gly>Glu
a-d3 164428004 G>A 0.99 Gly>Glu b2-d2 164428833 G>A 0.99 Gly>Glu
a-d5 164428010 G>A 0.99 Gly>Glu b3-a5 164428833 G>A 0.99 Gly>Glu
a1–a5 164423003 G>A 0.99 Glu>Lys c1-a1 164428617 C>T 0.99 Ser>Phe
a1-b3 164423003 G>A 0.99 Glu>Lys c1-a2 164423021 C>T 0.99 His>Tyr
a1-d1 164423109 C>T 0.99 Ser>Phe c1-a3 164428932 C>A 0.99 Ser>Stop
b1-a3 164423363 G>A 0.84* Splice site c1-a6 164427979 C>T 0.99 Gln>Stop
b1-a5 164423363 G>A 0.78** Splice site c1-b1 164428004 G>A 0.99 Gly>Glu
b1-a6 164423363 G>A 0.99 Splice site c1-c1 164423363 G>A 0.99 Splice site
b1–b5 164428596 G>A 0.99 Gly>Glu c1–c2 164423021 C>T 0.99 His>Tyr
b1-c1 164423363 G>A 0.99 Splice site c1–c6 164428617 C>T 0.99 Ser>Phe
b1-c6 164428009 G>A 0.99 Gly>Arg c1-d1 164423021 C>T 0.99 His>Tyr
b1-d2 164428596 G>A 0.99 Gly>Glu c1-d4 164428832 G>A 0.99 Gly>Arg
b1-d3 164428596 G>A 0.99 Gly>Glu c3-a4 164428004 G>A 0.99 Gly>Glu
b2-a1 164428670 C>T 0.99 Gln>Stop c3–c4 164427932 G>A 0.99 Splice site
b2-a4 164428009 G>A 0.99 Gly>Arg c3-d2 164427979 C>T 0.99 Gln>Stop
b2-b1 164428989 G>A 0.99 Trp>Stop L5178Y None --- None
*

A secondary mutation at 164428670 C>T (Gln>Stop, 0.16 frequency) was present in this clone.

This secondary mutation was found as a primary mutation in other clones.

**

A secondary mutation at 164428810 G>A (Splice site, 0.21 frequency) was present in this clone.

This secondary mutation was not found as a primary mutation in other clones.

Duplicate samples of this clone were submitted, both showed same results.