TABLE 2.
SNP locationb | Gene | Reference D/UW-3/CX |
D-EC |
D-LC |
|||
---|---|---|---|---|---|---|---|
Gene start position | Gene stop position | nt change | aa change | nt change | aa change | ||
30572 | CT025 | 29069 | 29941 | C → G | Thr → Ser | C → G | Thr → Ser |
55047 | CT049 | 54113 | 55585 | G → C | Gly → Ala | G → C | Gly → Ala |
55099 | CT049 | 54113 | 55585 | A → G | None | A → G | None |
152276 | CT135 | 152143 | 153225 | None | None | ΔT | Frameshift |
152686 | CT135 | 152143 | 153225 | ::T | Frameshift | None | None |
403784 | CT352 | 403499 | 403804 | A → C | Ile → Leu | A → C | Ile → Leu |
450477 | CT394 | 449841 | 451019 | A → G | Lys → Glu | A → G | Lys → Glu |
517109 | IGc (CT446-CT447) | 516946 | 519105 | G → T | None | G → T | None |
588168 | CT511 | 587942 | 588376 | G → T | Thr → Lys | G → T | Thr → Lys |
621054 | CT551 | 620037 | 621068 | ::G | Frameshift | ::G | Frameshift |
628883 | IG (CT556-CT557) | 628808 | 630414 | C → T | None | C → T | None |
706330 | CT621 | 704354 | 706852 | T → C | Thr → Ala | T → C | Thr → Ala |
717493 | CT630 | 717087 | 717770 | T → C | Gln → Arg | T → C | Gln → Arg |
720059 | IG (CT632-CT633) | 719973 | 721287 | A → T | None | A → T | None |
727542 | CT638 | 726792 | 727559 | ::G | Frameshift | ::G | Frameshift |
733706 | CT640 | 730899 | 733913 | T → C | Thr → Ala | T → C | Thr → Ala |
752502 | IG (CT655-CT656) | 752365 | 753143 | ::C | None | ::C | None |
858691 | 23S rRNA | 878039 | 880902 | G → A | None | G → A | None |
858694 | 23S rRNA | 878039 | 880902 | G → A | None | G → A | None |
858698 | 23S rRNA | 878039 | 880902 | ΔC | None | ΔC | None |
Boldface type indicates unique mutations identified in D-EC and D-LC. nt, nucleotide; aa, amino acid; ::, insertion; Δ, deletion.
SNP location refers to the location of the mutation in the reference D/UW-3/CX genome; for a single base pair insertion, the location of the preceding nucleotide is given.
IG, intergenic region and adjacent ORFs.