Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01230 | A08 | 874453 | C | T | missense_variant | MODERATE | c.1139G>A|p.Cys380Tyr |
S105 S106 |
2 | BAA08g01230 | A08 | 881913 | C | T | intron_variant | MODIFIER | c.280-2218G>A| |
S153 S213 |
3 | BAA08g01230 | A08 | 882555 | C | T | intron_variant | MODIFIER | c.280-2860G>A| |
S70 |
4 | BAA08g01230 | A08 | 884870 | C | T | intron_variant | MODIFIER | c.280-5175G>A| |
S294 |
5 | BAA08g01230 | A08 | 885638 | C | T | intron_variant | MODIFIER | c.280-5943G>A| |
S245 |
6 | BAA08g01230 | A08 | 886615 | C | T | intron_variant | MODIFIER | c.280-6920G>A| |
S163 |
7 | BAA08g01230 | A08 | 886721 | C | A | intron_variant | MODIFIER | c.280-7026G>T| |
S262 |
8 | BAA08g01230 | A08 | 886991 | G | A | intron_variant | MODIFIER | c.280-7296C>T| |
S32 |
9 | BAA08g01230 | A08 | 887657 | C | T | intron_variant | MODIFIER | c.279+7561G>A| |
S175 |
10 | BAA08g01230 | A08 | 891717 | C | T | intron_variant | MODIFIER | c.279+3501G>A| |
S305 |
11 | BAA08g01230 | A08 | 892428 | C | T | intron_variant | MODIFIER | c.279+2790G>A| |
S89 |
12 | BAA08g01230 | A08 | 892492 | G | A | intron_variant | MODIFIER | c.279+2726C>T| |
S217 |
13 | BAA08g01230 | A08 | 892662 | G | A | intron_variant | MODIFIER | c.279+2556C>T| |
S20 |
14 | BAA08g01230 | A08 | 898362 | C | T | missense_variant | MODERATE | c.20G>A|p.Gly7Glu |
S203 |
15 | BAA08g01230 | A08 | 899131 | G | A | upstream_gene_variant | MODIFIER | c.-750C>T| |
S95 |
16 | BAA08g01230 | A08 | 899223 | C | T | upstream_gene_variant | MODIFIER | c.-842G>A| |
S201 |
17 | BAA08g01230 | A08 | 901423 | C | T | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S163 |
18 | BAA08g01230 | A08 | 902153 | C | T | upstream_gene_variant | MODIFIER | c.-3772G>A| |
S80 |