Genotype (no. of strains) | Nucleotide change | Amino acid change | Accession number | |
---|---|---|---|---|
D (9) | D1 (7) | (129C → T, | (Synonymous, | LC498598 |
184G → A, | Val → Met, | |||
186 T → G, |  | |||
195C → T | Synonymous, | |||
636A → T)a | Synonymous)b | |||
D2 (1) | ()a + 977C → Ta | ()b +Ala→Val | LC498599 | |
D3 (1) | No mutations | Â | LC498600 | |
E (12) | Â | No mutations | Â | LC498601 |
F (25) | F1 (24) | No mutations | Â | LC498602 |
F2 (1) | 397C → A | Arg → Ser | LC498603 | |
Gc (6) | G1 (4) | 487G → A | Gly → Ser | LC498604 |
G2 (1) | 487G → A +  23 SNPs | Gly → Ser | LC498605 | |
H (4) |  | 272A → G | Asn → Ser | LC498606 |
850C → T | Synonymous | |||
I (2) | I1 (1) | 684G → A | Synonymous | LC498607 |
764 T → C | Ile → Thr | |||
810C → T | Synonymous | |||
1000 T → G | Ser → Ala | |||
1007C → G | Ala→Gly | |||
Insertion of codon AGC between 1008 and 1009 | Insertion of Gly | |||
1011A → T | Glu → Val | |||
1017A → C | Glu → Ala | |||
I2d (1) | 684G → A | Synonymous | LC498608 | |
764 T → C, | Ile → Thr | |||
810C → T, | Synonymous | |||
938C → T | Ala→Val | |||
J (1) |  | 369C → T | Synonymous | LC498609 |
K (2) |  | 293A → G | Asn → Ser | LC498610 |