Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g43480 | A02 | 36009981 | G | A | upstream_gene_variant | MODIFIER | c.-4209G>A| |
S207 |
2 | BAA02g43480 | A02 | 36010444 | C | T | upstream_gene_variant | MODIFIER | c.-3746C>T| |
S46 |
3 | BAA02g43480 | A02 | 36010483 | C | T | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S6 |
4 | BAA02g43480 | A02 | 36010758 | C | T | upstream_gene_variant | MODIFIER | c.-3432C>T| |
S104 S105 S52 |
5 | BAA02g43480 | A02 | 36010908 | C | T | upstream_gene_variant | MODIFIER | c.-3282C>T| |
S138 S181 |
6 | BAA02g43480 | A02 | 36011114 | C | T | upstream_gene_variant | MODIFIER | c.-3076C>T| |
S179 |
7 | BAA02g43480 | A02 | 36011746 | G | A | upstream_gene_variant | MODIFIER | c.-2444G>A| |
S177 |
8 | BAA02g43480 | A02 | 36011929 | C | T | upstream_gene_variant | MODIFIER | c.-2261C>T| |
S18 |
9 | BAA02g43480 | A02 | 36012037 | C | T | upstream_gene_variant | MODIFIER | c.-2153C>T| |
S182 |
10 | BAA02g43480 | A02 | 36012400 | C | A | upstream_gene_variant | MODIFIER | c.-1790C>A| |
S5 |
11 | BAA02g43480 | A02 | 36012649 | G | A | upstream_gene_variant | MODIFIER | c.-1541G>A| |
S37 |
12 | BAA02g43480 | A02 | 36012832 | C | T | upstream_gene_variant | MODIFIER | c.-1358C>T| |
S63 |
13 | BAA02g43480 | A02 | 36013087 | C | T | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S260 |
14 | BAA02g43480 | A02 | 36013980 | C | T | upstream_gene_variant | MODIFIER | c.-210C>T| |
S226 |
15 | BAA02g43480 | A02 | 36014386 | G | A | missense_variant | MODERATE | c.103G>A|p.Asp35Asn |
S84 S93 |
16 | BAA02g43480 | A02 | 36014790 | G | A | missense_variant | MODERATE | c.377G>A|p.Arg126Lys |
S298 |
17 | BAA02g43480 | A02 | 36016337 | C | T | missense_variant | MODERATE | c.728C>T|p.Ser243Phe |
S15 S153 S156 S213 S3 S34 S4 S6 |
18 | BAA02g43480 | A02 | 36016358 | C | T | missense_variant | MODERATE | c.749C>T|p.Thr250Ile |
S283 |
19 | BAA02g43480 | A02 | 36016974 | C | T | synonymous_variant | LOW | c.1204C>T|p.Leu402Leu |
S202 |