Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g36570 | A05 | 36551622 | G | A | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S25 |
2 | BAA05g36570 | A05 | 36551653 | A | T | missense_variant | MODERATE | c.35A>T|p.Asp12Val |
S155 S211 |
3 | BAA05g36570 | A05 | 36552351 | G | A | splice_region_variant&intron_variant | LOW | c.429+8G>A| |
S107 |
4 | BAA05g36570 | A05 | 36552777 | C | T | splice_region_variant&intron_variant | LOW | c.535-5C>T| |
S191 |
5 | BAA05g36570 | A05 | 36553075 | C | T | missense_variant | MODERATE | c.685C>T|p.Pro229Ser |
S65 |
6 | BAA05g36570 | A05 | 36553912 | C | T | splice_region_variant&intron_variant | LOW | c.1082+6C>T| |
S249 |
7 | BAA05g36570 | A05 | 36554380 | G | A | missense_variant | MODERATE | c.1198G>A|p.Gly400Arg |
S265 |
8 | BAA05g36570 | A05 | 36555598 | G | A | missense_variant&splice_region_variant | MODERATE | c.1739G>A|p.Gly580Glu |
S111 |
9 | BAA05g36570 | A05 | 36557768 | C | T | missense_variant | MODERATE | c.2498C>T|p.Ser833Phe |
S247 |
10 | BAA05g36570 | A05 | 36558976 | C | T | missense_variant | MODERATE | c.2924C>T|p.Ala975Val |
S140 |