Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14040 | A08 | 12055778 | C | T | missense_variant | MODERATE | c.28C>T|p.Pro10Ser |
S213 |
2 | BAA08g14040 | A08 | 12055831 | G | A | synonymous_variant | LOW | c.81G>A|p.Ala27Ala |
S282 |
3 | BAA08g14040 | A08 | 12055857 | G | A | missense_variant | MODERATE | c.107G>A|p.Arg36Lys |
S179 |
4 | BAA08g14040 | A08 | 12056017 | G | A | synonymous_variant | LOW | c.267G>A|p.Arg89Arg |
S15 S3 |
5 | BAA08g14040 | A08 | 12056089 | C | T | synonymous_variant | LOW | c.339C>T|p.Arg113Arg |
S143 |
6 | BAA08g14040 | A08 | 12056326 | G | A | synonymous_variant | LOW | c.576G>A|p.Leu192Leu |
S20 |
7 | BAA08g14040 | A08 | 12056400 | G | A | missense_variant | MODERATE | c.650G>A|p.Arg217Gln |
S190 |
8 | BAA08g14040 | A08 | 12056897 | G | A | synonymous_variant | LOW | c.1056G>A|p.Glu352Glu |
S281 |
9 | BAA08g14040 | A08 | 12056911 | G | A | missense_variant | MODERATE | c.1070G>A|p.Gly357Asp |
S58 |
10 | BAA08g14040 | A08 | 12058147 | G | A | missense_variant | MODERATE | c.1675G>A|p.Ala559Thr |
S202 |
11 | BAA08g14040 | A08 | 12058181 | C | T | missense_variant | MODERATE | c.1709C>T|p.Pro570Leu |
S79 S84 |
12 | BAA08g14040 | A08 | 12058193 | C | T | missense_variant | MODERATE | c.1721C>T|p.Pro574Leu |
S153 S213 |
13 | BAA08g14040 | A08 | 12059068 | G | A | stop_gained | HIGH | c.2408G>A|p.Trp803* |
S243 S299 |
14 | BAA08g14040 | A08 | 12059092 | G | A | missense_variant | MODERATE | c.2432G>A|p.Gly811Glu |
S10 |