Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01740 | A09 | 1223101 | G | A | missense_variant | MODERATE | c.188G>A|p.Gly63Asp |
S38 |
2 | BAA09g01740 | A09 | 1223190 | G | A | missense_variant | MODERATE | c.277G>A|p.Asp93Asn |
S210 S225 |
3 | BAA09g01740 | A09 | 1223336 | G | A | synonymous_variant | LOW | c.423G>A|p.Lys141Lys |
S125 |
4 | BAA09g01740 | A09 | 1223624 | C | T | synonymous_variant | LOW | c.711C>T|p.Ile237Ile |
S293 |
5 | BAA09g01740 | A09 | 1224111 | C | T | missense_variant | MODERATE | c.1198C>T|p.Pro400Ser |
S177 |
6 | BAA09g01740 | A09 | 1224132 | G | A | missense_variant | MODERATE | c.1219G>A|p.Ala407Thr |
S72 S78 |
7 | BAA09g01740 | A09 | 1224213 | C | T | missense_variant | MODERATE | c.1300C>T|p.Leu434Phe |
S171 |
8 | BAA09g01740 | A09 | 1224557 | G | A | synonymous_variant | LOW | c.1644G>A|p.Gln548Gln |
S293 |
9 | BAA09g01740 | A09 | 1224574 | C | T | missense_variant | MODERATE | c.1661C>T|p.Pro554Leu |
S206 |
10 | BAA09g01740 | A09 | 1224748 | C | T | missense_variant | MODERATE | c.1835C>T|p.Ala612Val |
S48 |
11 | BAA09g01740 | A09 | 1224806 | C | T | synonymous_variant | LOW | c.1893C>T|p.Asn631Asn |
S156 |
12 | BAA09g01740 | A09 | 1224819 | G | A | missense_variant | MODERATE | c.1906G>A|p.Ala636Thr |
S139 |
13 | BAA09g01740 | A09 | 1225038 | G | A | missense_variant | MODERATE | c.2125G>A|p.Glu709Lys |
S97 |
14 | BAA09g01740 | A09 | 1225482 | G | A | missense_variant | MODERATE | c.2569G>A|p.Ala857Thr |
S12 |
15 | BAA09g01740 | A09 | 1225895 | G | A | synonymous_variant | LOW | c.2982G>A|p.Lys994Lys |
S79 S84 |
16 | BAA09g01740 | A09 | 1226480 | A | C | synonymous_variant | LOW | c.3567A>C|p.Ser1189Ser |
S202 |
17 | BAA09g01740 | A09 | 1226576 | C | T | synonymous_variant | LOW | c.3663C>T|p.Leu1221Leu |
S212 |
18 | BAA09g01740 | A09 | 1226804 | C | T | synonymous_variant | LOW | c.3891C>T|p.Val1297Val |
S152 |