Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13810 | A08 | 11932631 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S235 |
2 | BAA08g13810 | A08 | 11933177 | C | T | synonymous_variant | LOW | c.532C>T|p.Leu178Leu |
S294 |
3 | BAA08g13810 | A08 | 11933840 | C | T | missense_variant | MODERATE | c.919C>T|p.Leu307Phe |
S177 |
4 | BAA08g13810 | A08 | 11934764 | C | T | synonymous_variant | LOW | c.1527C>T|p.Tyr509Tyr |
S197 |
5 | BAA08g13810 | A08 | 11935238 | C | T | stop_gained | HIGH | c.1726C>T|p.Arg576* |
S67 |
6 | BAA08g13810 | A08 | 11935357 | C | T | synonymous_variant | LOW | c.1845C>T|p.His615His |
S135 |
7 | BAA08g13810 | A08 | 11935475 | C | T | stop_gained | HIGH | c.1963C>T|p.Arg655* |
S17 |
8 | BAA08g13810 | A08 | 11936548 | G | A | synonymous_variant | LOW | c.2904G>A|p.Arg968Arg |
S32 |
9 | BAA08g13810 | A08 | 11936740 | G | A | missense_variant | MODERATE | c.2992G>A|p.Ala998Thr |
S130 |
10 | BAA08g13810 | A08 | 11937096 | C | T | downstream_gene_variant | MODIFIER | c.*306C>T| |
S280 |