Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13650 | A08 | 11841783 | C | T | upstream_gene_variant | MODIFIER | c.-4741C>T| |
S177 |
2 | BAA08g13650 | A08 | 11841915 | C | T | upstream_gene_variant | MODIFIER | c.-4609C>T| |
S50 |
3 | BAA08g13650 | A08 | 11842054 | G | A | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S190 |
4 | BAA08g13650 | A08 | 11842136 | C | T | upstream_gene_variant | MODIFIER | c.-4388C>T| |
S219 |
5 | BAA08g13650 | A08 | 11842344 | G | A | upstream_gene_variant | MODIFIER | c.-4180G>A| |
S66 |
6 | BAA08g13650 | A08 | 11843054 | C | T | upstream_gene_variant | MODIFIER | c.-3470C>T| |
S178 |
7 | BAA08g13650 | A08 | 11843279 | G | A | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S90 |
8 | BAA08g13650 | A08 | 11843794 | G | A | upstream_gene_variant | MODIFIER | c.-2730G>A| |
S202 |
9 | BAA08g13650 | A08 | 11844615 | C | T | upstream_gene_variant | MODIFIER | c.-1909C>T| |
S7 |
10 | BAA08g13650 | A08 | 11844882 | G | A | upstream_gene_variant | MODIFIER | c.-1642G>A| |
S140 |
11 | BAA08g13650 | A08 | 11845370 | C | T | upstream_gene_variant | MODIFIER | c.-1154C>T| |
S208 |
12 | BAA08g13650 | A08 | 11848508 | G | A | intron_variant | MODIFIER | c.467+1518G>A| |
S266 |
13 | BAA08g13650 | A08 | 11849454 | C | T | intron_variant | MODIFIER | c.467+2464C>T| |
S104 S52 |
14 | BAA08g13650 | A08 | 11850367 | C | T | intron_variant | MODIFIER | c.467+3377C>T| |
S126 |
15 | BAA08g13650 | A08 | 11850616 | G | A | intron_variant | MODIFIER | c.467+3626G>A| |
S127 |
16 | BAA08g13650 | A08 | 11855090 | C | T | intron_variant | MODIFIER | c.468-3216C>T| |
S61 |
17 | BAA08g13650 | A08 | 11856322 | C | T | intron_variant | MODIFIER | c.468-1984C>T| |
S126 |
18 | BAA08g13650 | A08 | 11856507 | G | A | intron_variant | MODIFIER | c.468-1799G>A| |
S172 S217 |
19 | BAA08g13650 | A08 | 11856895 | C | T | intron_variant | MODIFIER | c.468-1411C>T| |
S177 |
20 | BAA08g13650 | A08 | 11857107 | C | T | intron_variant | MODIFIER | c.468-1199C>T| |
S160 |
21 | BAA08g13650 | A08 | 11857299 | C | T | intron_variant | MODIFIER | c.468-1007C>T| |
S303 |
22 | BAA08g13650 | A08 | 11857344 | C | T | intron_variant | MODIFIER | c.468-962C>T| |
S112 |
23 | BAA08g13650 | A08 | 11857627 | G | A | intron_variant | MODIFIER | c.468-679G>A| |
S35 |
24 | BAA08g13650 | A08 | 11857738 | C | T | intron_variant | MODIFIER | c.468-568C>T| |
S201 |
25 | BAA08g13650 | A08 | 11858544 | G | A | missense_variant | MODERATE | c.706G>A|p.Gly236Ser |
S250 |