Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g43240 | A09 | 49381922 | G | A | missense_variant | MODERATE | c.520G>A|p.Ala174Thr |
S105 S106 |
2 | BAA09g43240 | A09 | 49382358 | C | T | missense_variant | MODERATE | c.737C>T|p.Ser246Leu |
S180 |
3 | BAA09g43240 | A09 | 49386202 | G | A | missense_variant | MODERATE | c.2402G>A|p.Arg801Gln |
S167 |
4 | BAA09g43240 | A09 | 49386247 | C | T | missense_variant | MODERATE | c.2447C>T|p.Ser816Leu |
S56 |
5 | BAA09g43240 | A09 | 49387208 | G | A | synonymous_variant | LOW | c.3108G>A|p.Ala1036Ala |
S128 |
6 | BAA09g43240 | A09 | 49387730 | C | T | synonymous_variant | LOW | c.3630C>T|p.Asn1210Asn |
S148 S166 |
7 | BAA09g43240 | A09 | 49388131 | C | T | missense_variant | MODERATE | c.3922C>T|p.Pro1308Ser |
S277 |
8 | BAA09g43240 | A09 | 49388240 | C | T | missense_variant | MODERATE | c.4031C>T|p.Ala1344Val |
S223 |
9 | BAA09g43240 | A09 | 49388257 | G | A | missense_variant | MODERATE | c.4048G>A|p.Gly1350Arg |
S210 S225 |
10 | BAA09g43240 | A09 | 49388482 | G | A | missense_variant | MODERATE | c.4195G>A|p.Ala1399Thr |
S247 |
11 | BAA09g43240 | A09 | 49388814 | G | A | missense_variant | MODERATE | c.4527G>A|p.Met1509Ile |
S288 |
12 | BAA09g43240 | A09 | 49391137 | C | T | downstream_gene_variant | MODIFIER | c.*2260C>T| |
S121 |
13 | BAA09g43240 | A09 | 49391223 | C | T | downstream_gene_variant | MODIFIER | c.*2346C>T| |
S33 |
14 | BAA09g43240 | A09 | 49392491 | G | A | downstream_gene_variant | MODIFIER | c.*3614G>A| |
S284 |
15 | BAA09g43240 | A09 | 49392903 | C | T | downstream_gene_variant | MODIFIER | c.*4026C>T| |
S61 |