Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g25980 | A09 | 16778228 | G | A | downstream_gene_variant | MODIFIER | c.*2985C>T| |
S251 |
2 | BAA09g25980 | A09 | 16779733 | C | T | downstream_gene_variant | MODIFIER | c.*1480G>A| |
S36 |
3 | BAA09g25980 | A09 | 16780008 | G | A | downstream_gene_variant | MODIFIER | c.*1205C>T| |
S161 S244 S289 S290 |
4 | BAA09g25980 | A09 | 16780167 | C | T | downstream_gene_variant | MODIFIER | c.*1046G>A| |
S93 |
5 | BAA09g25980 | A09 | 16780688 | G | A | downstream_gene_variant | MODIFIER | c.*525C>T| |
S25 |
6 | BAA09g25980 | A09 | 16780991 | C | T | downstream_gene_variant | MODIFIER | c.*222G>A| |
S99 |
7 | BAA09g25980 | A09 | 16781671 | G | A | missense_variant | MODERATE | c.820C>T|p.Pro274Ser |
S201 |
8 | BAA09g25980 | A09 | 16781696 | C | T | synonymous_variant | LOW | c.795G>A|p.Pro265Pro |
S135 |
9 | BAA09g25980 | A09 | 16781704 | C | T | missense_variant | MODERATE | c.787G>A|p.Val263Ile |
S132 S137 |
10 | BAA09g25980 | A09 | 16781860 | G | A | missense_variant | MODERATE | c.631C>T|p.Pro211Ser |
S98 |
11 | BAA09g25980 | A09 | 16782152 | G | A | synonymous_variant | LOW | c.339C>T|p.Arg113Arg |
S33 |
12 | BAA09g25980 | A09 | 16782849 | C | T | upstream_gene_variant | MODIFIER | c.-263G>A| |
S28 |
13 | BAA09g25980 | A09 | 16783283 | C | T | upstream_gene_variant | MODIFIER | c.-697G>A| |
S161 |
14 | BAA09g25980 | A09 | 16784657 | G | A | upstream_gene_variant | MODIFIER | c.-2071C>T| |
S209 |
15 | BAA09g25980 | A09 | 16785156 | G | A | upstream_gene_variant | MODIFIER | c.-2570C>T| |
S236 |
16 | BAA09g25980 | A09 | 16785528 | G | A | upstream_gene_variant | MODIFIER | c.-2942C>T| |
S292 |
17 | BAA09g25980 | A09 | 16785707 | C | T | upstream_gene_variant | MODIFIER | c.-3121G>A| |
S108 |
18 | BAA09g25980 | A09 | 16785828 | C | T | upstream_gene_variant | MODIFIER | c.-3242G>A| |
S148 S210 |