Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g24590 | A09 | 15753649 | C | T | downstream_gene_variant | MODIFIER | c.*4978G>A| |
S118 |
2 | BAA09g24590 | A09 | 15753737 | G | A | downstream_gene_variant | MODIFIER | c.*4890C>T| |
S75 S81 |
3 | BAA09g24590 | A09 | 15753760 | C | T | downstream_gene_variant | MODIFIER | c.*4867G>A| |
S134 |
4 | BAA09g24590 | A09 | 15753803 | G | A | downstream_gene_variant | MODIFIER | c.*4824C>T| |
S301 |
5 | BAA09g24590 | A09 | 15753822 | G | A | downstream_gene_variant | MODIFIER | c.*4805C>T| |
S247 |
6 | BAA09g24590 | A09 | 15754487 | C | T | downstream_gene_variant | MODIFIER | c.*4140G>A| |
S182 |
7 | BAA09g24590 | A09 | 15754993 | G | A | downstream_gene_variant | MODIFIER | c.*3634C>T| |
S204 |
8 | BAA09g24590 | A09 | 15755391 | G | A | downstream_gene_variant | MODIFIER | c.*3236C>T| |
S106 |
9 | BAA09g24590 | A09 | 15756191 | G | A | downstream_gene_variant | MODIFIER | c.*2436C>T| |
S230 |
10 | BAA09g24590 | A09 | 15756474 | G | A | downstream_gene_variant | MODIFIER | c.*2153C>T| |
S295 |
11 | BAA09g24590 | A09 | 15758787 | C | T | missense_variant | MODERATE | c.2393G>A|p.Gly798Glu |
S242 |
12 | BAA09g24590 | A09 | 15762219 | G | A | missense_variant | MODERATE | c.1283C>T|p.Ser428Phe |
S265 S39 |
13 | BAA09g24590 | A09 | 15762266 | G | A | synonymous_variant | LOW | c.1236C>T|p.Asp412Asp |
S86 |
14 | BAA09g24590 | A09 | 15763519 | C | T | intron_variant | MODIFIER | c.1107-1124G>A| |
S228 |
15 | BAA09g24590 | A09 | 15765247 | G | A | intron_variant | MODIFIER | c.1106+2019C>T| |
S152 |
16 | BAA09g24590 | A09 | 15765894 | G | A | intron_variant | MODIFIER | c.1106+1372C>T| |
S75 S81 |
17 | BAA09g24590 | A09 | 15766113 | G | A | intron_variant | MODIFIER | c.1106+1153C>T| |
S149 |
18 | BAA09g24590 | A09 | 15766202 | G | A | intron_variant | MODIFIER | c.1106+1064C>T| |
S274 |
19 | BAA09g24590 | A09 | 15766597 | G | A | intron_variant | MODIFIER | c.1106+669C>T| |
S172 S217 |
20 | BAA09g24590 | A09 | 15766750 | C | T | intron_variant | MODIFIER | c.1106+516G>A| |
S239 |
21 | BAA09g24590 | A09 | 15766772 | G | A | intron_variant | MODIFIER | c.1106+494C>T| |
S163 |
22 | BAA09g24590 | A09 | 15767361 | C | T | synonymous_variant | LOW | c.1011G>A|p.Glu337Glu |
S278 |
23 | BAA09g24590 | A09 | 15767465 | G | A | intron_variant | MODIFIER | c.974-67C>T| |
S172 |
24 | BAA09g24590 | A09 | 15767758 | G | A | intron_variant | MODIFIER | c.974-360C>T| |
S244 |
25 | BAA09g24590 | A09 | 15767811 | G | A | intron_variant | MODIFIER | c.973+368C>T| |
S162 |