Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15160 | A04 | 20035289 | G | A | downstream_gene_variant | MODIFIER | c.*4520C>T| |
S150 |
2 | BAA04g15160 | A04 | 20035291 | G | A | downstream_gene_variant | MODIFIER | c.*4518C>T| |
S19 |
3 | BAA04g15160 | A04 | 20035663 | C | T | downstream_gene_variant | MODIFIER | c.*4146G>A| |
S55 |
4 | BAA04g15160 | A04 | 20036560 | G | A | downstream_gene_variant | MODIFIER | c.*3249C>T| |
S60 |
5 | BAA04g15160 | A04 | 20036834 | G | A | downstream_gene_variant | MODIFIER | c.*2975C>T| |
S75 S81 |
6 | BAA04g15160 | A04 | 20039165 | G | A | downstream_gene_variant | MODIFIER | c.*644C>T| |
S11 |
7 | BAA04g15160 | A04 | 20039877 | C | T | missense_variant | MODERATE | c.604G>A|p.Val202Ile |
S295 |
8 | BAA04g15160 | A04 | 20039892 | G | A | missense_variant | MODERATE | c.589C>T|p.Pro197Ser |
S166 |
9 | BAA04g15160 | A04 | 20040027 | C | T | missense_variant | MODERATE | c.454G>A|p.Val152Ile |
S110 |
10 | BAA04g15160 | A04 | 20040574 | C | T | missense_variant | MODERATE | c.16G>A|p.Ala6Thr |
S202 |
11 | BAA04g15160 | A04 | 20040620 | C | T | upstream_gene_variant | MODIFIER | c.-31G>A| |
S242 |
12 | BAA04g15160 | A04 | 20040654 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S35 |
13 | BAA04g15160 | A04 | 20041790 | G | A | upstream_gene_variant | MODIFIER | c.-1201C>T| |
S288 |
14 | BAA04g15160 | A04 | 20042123 | C | T | upstream_gene_variant | MODIFIER | c.-1534G>A| |
S111 |
15 | BAA04g15160 | A04 | 20042327 | G | A | upstream_gene_variant | MODIFIER | c.-1738C>T| |
S15 S3 |
16 | BAA04g15160 | A04 | 20044853 | G | A | upstream_gene_variant | MODIFIER | c.-4264C>T| |
S193 |
17 | BAA04g15160 | A04 | 20045202 | G | A | upstream_gene_variant | MODIFIER | c.-4613C>T| |
S59 |
18 | BAA04g15160 | A04 | 20045571 | G | A | upstream_gene_variant | MODIFIER | c.-4982C>T| |
S266 |