Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41180 | A09 | 48015959 | C | T | upstream_gene_variant | MODIFIER | c.-4982C>T| |
S202 |
2 | BAA09g41180 | A09 | 48016002 | G | A | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S47 |
3 | BAA09g41180 | A09 | 48016025 | C | T | upstream_gene_variant | MODIFIER | c.-4916C>T| |
S9 |
4 | BAA09g41180 | A09 | 48016543 | G | A | upstream_gene_variant | MODIFIER | c.-4398G>A| |
S207 |
5 | BAA09g41180 | A09 | 48016569 | C | T | upstream_gene_variant | MODIFIER | c.-4372C>T| |
S37 |
6 | BAA09g41180 | A09 | 48017401 | C | T | upstream_gene_variant | MODIFIER | c.-3540C>T| |
S103 |
7 | BAA09g41180 | A09 | 48018683 | C | T | upstream_gene_variant | MODIFIER | c.-2258C>T| |
S279 |
8 | BAA09g41180 | A09 | 48021152 | G | A | missense_variant | MODERATE | c.212G>A|p.Arg71Lys |
S75 S81 |
9 | BAA09g41180 | A09 | 48021294 | C | T | synonymous_variant | LOW | c.354C>T|p.Arg118Arg |
S208 S93 |
10 | BAA09g41180 | A09 | 48021796 | C | T | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S292 |
11 | BAA09g41180 | A09 | 48021914 | G | T | missense_variant | MODERATE | c.974G>T|p.Gly325Val |
S202 |
12 | BAA09g41180 | A09 | 48021923 | C | T | missense_variant | MODERATE | c.983C>T|p.Ser328Phe |
S94 |
13 | BAA09g41180 | A09 | 48021991 | G | A | missense_variant | MODERATE | c.1051G>A|p.Ala351Thr |
S170 |
14 | BAA09g41180 | A09 | 48022040 | G | A | missense_variant | MODERATE | c.1100G>A|p.Gly367Glu |
S252 |
15 | BAA09g41180 | A09 | 48022860 | G | A | downstream_gene_variant | MODIFIER | c.*297G>A| |
S39 |
16 | BAA09g41180 | A09 | 48023494 | G | A | downstream_gene_variant | MODIFIER | c.*931G>A| |
S187 |
17 | BAA09g41180 | A09 | 48023702 | G | A | downstream_gene_variant | MODIFIER | c.*1139G>A| |
S233 |
18 | BAA09g41180 | A09 | 48023776 | G | A | downstream_gene_variant | MODIFIER | c.*1213G>A| |
S231 |
19 | BAA09g41180 | A09 | 48023989 | C | T | downstream_gene_variant | MODIFIER | c.*1426C>T| |
S245 |
20 | BAA09g41180 | A09 | 48023999 | G | A | downstream_gene_variant | MODIFIER | c.*1436G>A| |
S196 |
21 | BAA09g41180 | A09 | 48024223 | C | T | downstream_gene_variant | MODIFIER | c.*1660C>T| |
S80 |