Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18070 | A05 | 10291999 | G | A | upstream_gene_variant | MODIFIER | c.-4542G>A| |
S75 S81 |
2 | BAA05g18070 | A05 | 10293769 | C | T | upstream_gene_variant | MODIFIER | c.-2772C>T| |
S242 |
3 | BAA05g18070 | A05 | 10294037 | G | A | upstream_gene_variant | MODIFIER | c.-2504G>A| |
S100 |
4 | BAA05g18070 | A05 | 10294653 | G | A | upstream_gene_variant | MODIFIER | c.-1888G>A| |
S264 |
5 | BAA05g18070 | A05 | 10295141 | C | T | upstream_gene_variant | MODIFIER | c.-1400C>T| |
S233 |
6 | BAA05g18070 | A05 | 10296513 | G | A | upstream_gene_variant | MODIFIER | c.-28G>A| |
S4 |
7 | BAA05g18070 | A05 | 10296563 | G | A | missense_variant | MODERATE | c.23G>A|p.Gly8Glu |
S77 |
8 | BAA05g18070 | A05 | 10296572 | G | A | missense_variant | MODERATE | c.32G>A|p.Gly11Glu |
S205 |
9 | BAA05g18070 | A05 | 10296820 | C | T | missense_variant | MODERATE | c.280C>T|p.Pro94Ser |
S28 |
10 | BAA05g18070 | A05 | 10297117 | G | A | synonymous_variant | LOW | c.438G>A|p.Ser146Ser |
S139 |
11 | BAA05g18070 | A05 | 10297284 | C | T | missense_variant | MODERATE | c.605C>T|p.Thr202Ile |
S103 |
12 | BAA05g18070 | A05 | 10297409 | C | T | synonymous_variant | LOW | c.730C>T|p.Leu244Leu |
S83 S88 |
13 | BAA05g18070 | A05 | 10297461 | C | T | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S169 |
14 | BAA05g18070 | A05 | 10297725 | G | A | missense_variant | MODERATE | c.1046G>A|p.Gly349Asp |
S274 |
15 | BAA05g18070 | A05 | 10297853 | G | A | missense_variant | MODERATE | c.1174G>A|p.Glu392Lys |
S151 S263 |
16 | BAA05g18070 | A05 | 10298585 | C | T | missense_variant | MODERATE | c.1906C>T|p.Leu636Phe |
S50 |
17 | BAA05g18070 | A05 | 10298595 | C | T | missense_variant | MODERATE | c.1916C>T|p.Ala639Val |
S181 |
18 | BAA05g18070 | A05 | 10298766 | C | T | missense_variant | MODERATE | c.2087C>T|p.Thr696Ile |
S251 |
19 | BAA05g18070 | A05 | 10298973 | C | T | missense_variant | MODERATE | c.2294C>T|p.Thr765Ile |
S87 |
20 | BAA05g18070 | A05 | 10299018 | C | T | missense_variant | MODERATE | c.2339C>T|p.Ala780Val |
S8 |
21 | BAA05g18070 | A05 | 10299219 | C | T | missense_variant | MODERATE | c.2540C>T|p.Pro847Leu |
S58 |
22 | BAA05g18070 | A05 | 10299493 | C | T | synonymous_variant | LOW | c.2814C>T|p.Arg938Arg |
S289 S290 |
23 | BAA05g18070 | A05 | 10299709 | C | T | synonymous_variant | LOW | c.3030C>T|p.Val1010Val |
S229 |
24 | BAA05g18070 | A05 | 10301540 | C | T | downstream_gene_variant | MODIFIER | c.*1828C>T| |
S133 |
25 | BAA05g18070 | A05 | 10304443 | C | T | downstream_gene_variant | MODIFIER | c.*4731C>T| |
S113 |