Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g42050 | A07 | 36659281 | A | C | missense_variant | MODERATE | c.2833T>G|p.Ser945Ala |
S232 |
2 | BAA07g42050 | A07 | 36659349 | G | A | missense_variant | MODERATE | c.2765C>T|p.Thr922Ile |
S183 S198 |
3 | BAA07g42050 | A07 | 36659476 | C | T | missense_variant | MODERATE | c.2638G>A|p.Ala880Thr |
S260 |
4 | BAA07g42050 | A07 | 36659573 | G | A | synonymous_variant | LOW | c.2541C>T|p.His847His |
S186 |
5 | BAA07g42050 | A07 | 36662359 | C | T | missense_variant | MODERATE | c.887G>A|p.Arg296Lys |
S262 |
6 | BAA07g42050 | A07 | 36664956 | C | T | upstream_gene_variant | MODIFIER | c.-1172G>A| |
S107 |
7 | BAA07g42050 | A07 | 36665352 | G | A | upstream_gene_variant | MODIFIER | c.-1568C>T| |
S194 |
8 | BAA07g42050 | A07 | 36665443 | G | A | upstream_gene_variant | MODIFIER | c.-1659C>T| |
S5 |
9 | BAA07g42050 | A07 | 36666642 | G | A | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S171 |
10 | BAA07g42050 | A07 | 36667100 | C | T | upstream_gene_variant | MODIFIER | c.-3316G>A| |
S15 S190 |
11 | BAA07g42050 | A07 | 36668195 | G | A | upstream_gene_variant | MODIFIER | c.-4411C>T| |
S134 |
12 | BAA07g42050 | A07 | 36668612 | G | A | upstream_gene_variant | MODIFIER | c.-4828C>T| |
S130 |
13 | BAA07g42050 | A07 | 36668630 | G | A | upstream_gene_variant | MODIFIER | c.-4846C>T| |
S185 S203 S273 |