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. 2010 Jun;185(2):479–495. doi: 10.1534/genetics.110.117259

TABLE 3.

The nature and location of mutations found in this study

Gene Sequenced mutant line Nucleotide changes Amino acid changes Location of mutation
CG41265 (l(2)41Ab) EMS45-10 G → A (W → stop) +93785 (exon 7)
CG42595 (uex) L2 C → T Q → STOP +10139 (exon 4)
NC1 13-bp deletion and 4-bp deletion frameshift + possible loss of a splice junction motif +9949 to +9961 (exon 11) and +9989 to +9991 (intron 11)
uex34-7 G → C M → I +3 (putative transcription start site)
CG17683 NC109 T → A and T → G V → D and S → A +559 and +564 (exon 3)
NC38 T → A C → STOP +602 (exon 3)
EMS 34-13 C → T S → F +658 (exon 3)
CG40127 NC110 T → A L → H +375 (exon 3)
CG17665 EMS 45-34 G → A W → STOP +3917 (exon 3)
EMS 45-61 C → T R → STOP +6088 (exon 7)
EMS 45-71 G → A G → E +4168 (exon 3)
NC19 G → A W → STOP +3736 (exon 3)
NC28 T → A L → P +3796 (exon 3)

Genes are listed in the proximal to distal direction. The location of the mutation is written as the number of amino acids downstream (+) or upstream (−) from the predicted translation start site (+0).