Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g27770 | A01 | 16765113 | G | A | upstream_gene_variant | MODIFIER | c.-4863G>A| |
S172 |
2 | BAA01g27770 | A01 | 16765249 | G | A | upstream_gene_variant | MODIFIER | c.-4727G>A| |
S284 |
3 | BAA01g27770 | A01 | 16765585 | G | A | upstream_gene_variant | MODIFIER | c.-4391G>A| |
S187 |
4 | BAA01g27770 | A01 | 16765680 | C | T | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S42 |
5 | BAA01g27770 | A01 | 16766708 | C | T | upstream_gene_variant | MODIFIER | c.-3268C>T| |
S185 |
6 | BAA01g27770 | A01 | 16766806 | C | T | upstream_gene_variant | MODIFIER | c.-3170C>T| |
S134 |
7 | BAA01g27770 | A01 | 16766816 | G | A | upstream_gene_variant | MODIFIER | c.-3160G>A| |
S199 |
8 | BAA01g27770 | A01 | 16766832 | C | T | upstream_gene_variant | MODIFIER | c.-3144C>T| |
S148 S30 S31 |
9 | BAA01g27770 | A01 | 16767230 | G | A | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S74 |
10 | BAA01g27770 | A01 | 16767236 | C | T | upstream_gene_variant | MODIFIER | c.-2740C>T| |
S139 |
11 | BAA01g27770 | A01 | 16767276 | G | A | upstream_gene_variant | MODIFIER | c.-2700G>A| |
S292 |
12 | BAA01g27770 | A01 | 16769691 | G | A | upstream_gene_variant | MODIFIER | c.-285G>A| |
S181 |
13 | BAA01g27770 | A01 | 16769702 | C | T | upstream_gene_variant | MODIFIER | c.-274C>T| |
S286 |
14 | BAA01g27770 | A01 | 16770208 | G | A | missense_variant | MODERATE | c.145G>A|p.Val49Met |
S138 |
15 | BAA01g27770 | A01 | 16770276 | C | T | synonymous_variant | LOW | c.213C>T|p.Cys71Cys |
S46 |
16 | BAA01g27770 | A01 | 16770370 | C | T | missense_variant | MODERATE | c.307C>T|p.Leu103Phe |
S282 |
17 | BAA01g27770 | A01 | 16770426 | C | T | synonymous_variant | LOW | c.363C>T|p.Tyr121Tyr |
S282 |
18 | BAA01g27770 | A01 | 16770777 | A | T | missense_variant | MODERATE | c.714A>T|p.Glu238Asp |
S159 S243 |
19 | BAA01g27770 | A01 | 16771132 | G | A | missense_variant | MODERATE | c.910G>A|p.Val304Ile |
S32 |
20 | BAA01g27770 | A01 | 16771638 | C | T | missense_variant | MODERATE | c.1352C>T|p.Thr451Ile |
S242 |
21 | BAA01g27770 | A01 | 16771879 | C | T | missense_variant | MODERATE | c.1478C>T|p.Ser493Phe |
S303 |
22 | BAA01g27770 | A01 | 16771889 | C | T | synonymous_variant | LOW | c.1488C>T|p.His496His |
S69 |
23 | BAA01g27770 | A01 | 16771948 | A | G | missense_variant | MODERATE | c.1547A>G|p.Asn516Ser |
S257 |
24 | BAA01g27770 | A01 | 16772240 | C | T | missense_variant | MODERATE | c.1724C>T|p.Ser575Phe |
S48 |
25 | BAA01g27770 | A01 | 16772293 | C | T | missense_variant | MODERATE | c.1777C>T|p.His593Tyr |
S10 |