Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19260 | A01 | 9474970 | G | A | downstream_gene_variant | MODIFIER | c.*1706C>T| |
S142 |
2 | BAA01g19260 | A01 | 9474985 | G | A | downstream_gene_variant | MODIFIER | c.*1691C>T| |
S12 |
3 | BAA01g19260 | A01 | 9475040 | C | T | downstream_gene_variant | MODIFIER | c.*1636G>A| |
S130 |
4 | BAA01g19260 | A01 | 9475046 | C | T | downstream_gene_variant | MODIFIER | c.*1630G>A| |
S134 |
5 | BAA01g19260 | A01 | 9476723 | G | A | splice_region_variant&intron_variant | LOW | c.2794-6C>T| |
S109 |
6 | BAA01g19260 | A01 | 9476851 | C | T | missense_variant | MODERATE | c.2746G>A|p.Val916Ile |
S118 |
7 | BAA01g19260 | A01 | 9476874 | G | A | missense_variant | MODERATE | c.2723C>T|p.Ser908Phe |
S195 |
8 | BAA01g19260 | A01 | 9478006 | G | A | synonymous_variant | LOW | c.1854C>T|p.Leu618Leu |
S280 |
9 | BAA01g19260 | A01 | 9478037 | G | A | missense_variant | MODERATE | c.1823C>T|p.Ser608Phe |
S245 |
10 | BAA01g19260 | A01 | 9478687 | G | A | synonymous_variant | LOW | c.1173C>T|p.Leu391Leu |
S165 |
11 | BAA01g19260 | A01 | 9478835 | C | T | missense_variant | MODERATE | c.1025G>A|p.Gly342Glu |
S146 |
12 | BAA01g19260 | A01 | 9479442 | C | A | stop_gained | HIGH | c.418G>T|p.Glu140* |
S64 |
13 | BAA01g19260 | A01 | 9479747 | A | C | missense_variant | MODERATE | c.113T>G|p.Leu38Arg |
S173 S265 S289 |
14 | BAA01g19260 | A01 | 9479899 | C | T | upstream_gene_variant | MODIFIER | c.-40G>A| |
S155 S211 |
15 | BAA01g19260 | A01 | 9482117 | C | T | upstream_gene_variant | MODIFIER | c.-2258G>A| |
S62 |
16 | BAA01g19260 | A01 | 9482302 | G | A | upstream_gene_variant | MODIFIER | c.-2443C>T| |
S95 |
17 | BAA01g19260 | A01 | 9482365 | G | A | upstream_gene_variant | MODIFIER | c.-2506C>T| |
S126 |
18 | BAA01g19260 | A01 | 9484495 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S103 |
19 | BAA01g19260 | A01 | 9484753 | G | A | upstream_gene_variant | MODIFIER | c.-4894C>T| |
S224 |