Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g16990 | A03 | 7425284 | G | A | missense_variant | MODERATE | c.1870C>T|p.Pro624Ser |
S10 |
2 | BAA03g16990 | A03 | 7425788 | C | T | missense_variant | MODERATE | c.1366G>A|p.Glu456Lys |
S263 |
3 | BAA03g16990 | A03 | 7426293 | G | A | synonymous_variant | LOW | c.861C>T|p.Ala287Ala |
S280 |
4 | BAA03g16990 | A03 | 7426629 | G | A | missense_variant | MODERATE | c.604C>T|p.Pro202Ser |
S168 S219 S278 S279 S64 S72 |
5 | BAA03g16990 | A03 | 7426778 | C | T | missense_variant | MODERATE | c.455G>A|p.Arg152His |
S293 |
6 | BAA03g16990 | A03 | 7426823 | G | A | missense_variant | MODERATE | c.410C>T|p.Thr137Ile |
S144 |
7 | BAA03g16990 | A03 | 7428058 | G | A | upstream_gene_variant | MODIFIER | c.-826C>T| |
S44 |
8 | BAA03g16990 | A03 | 7428121 | G | A | upstream_gene_variant | MODIFIER | c.-889C>T| |
S128 |
9 | BAA03g16990 | A03 | 7428688 | G | A | upstream_gene_variant | MODIFIER | c.-1456C>T| |
S185 |
10 | BAA03g16990 | A03 | 7430847 | C | T | upstream_gene_variant | MODIFIER | c.-3615G>A| |
S134 |
11 | BAA03g16990 | A03 | 7431031 | C | T | upstream_gene_variant | MODIFIER | c.-3799G>A| |
S266 |
12 | BAA03g16990 | A03 | 7431122 | G | A | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S50 |