Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09520 | A02 | 4191500 | G | A | synonymous_variant | LOW | c.4300C>T|p.Leu1434Leu |
S223 |
2 | BAA02g09520 | A02 | 4192353 | C | T | synonymous_variant | LOW | c.3900G>A|p.Leu1300Leu |
S286 |
3 | BAA02g09520 | A02 | 4192505 | G | A | missense_variant | MODERATE | c.3853C>T|p.Leu1285Phe |
S209 |
4 | BAA02g09520 | A02 | 4193442 | G | A | missense_variant | MODERATE | c.3277C>T|p.Leu1093Phe |
S188 |
5 | BAA02g09520 | A02 | 4193755 | C | T | missense_variant | MODERATE | c.3139G>A|p.Val1047Ile |
S121 |
6 | BAA02g09520 | A02 | 4194278 | G | A | missense_variant | MODERATE | c.2879C>T|p.Pro960Leu |
S34 |
7 | BAA02g09520 | A02 | 4195912 | C | T | intron_variant | MODIFIER | c.1962+14G>A| |
S242 |
8 | BAA02g09520 | A02 | 4196163 | C | T | intron_variant | MODIFIER | c.1830+74G>A| |
S245 |
9 | BAA02g09520 | A02 | 4199050 | G | A | missense_variant | MODERATE | c.407C>T|p.Ala136Val |
S50 |
10 | BAA02g09520 | A02 | 4201549 | C | T | upstream_gene_variant | MODIFIER | c.-1083G>A| |
S219 S72 |
11 | BAA02g09520 | A02 | 4203690 | G | A | upstream_gene_variant | MODIFIER | c.-3224C>T| |
S98 |
12 | BAA02g09520 | A02 | 4204835 | G | A | upstream_gene_variant | MODIFIER | c.-4369C>T| |
S45 |
13 | BAA02g09520 | A02 | 4205320 | T | A | upstream_gene_variant | MODIFIER | c.-4854A>T| |
S266 |
14 | BAA02g09520 | A02 | 4205428 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S178 |