Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11350 | A04 | 17283475 | G | A | upstream_gene_variant | MODIFIER | c.-4449G>A| |
S116 |
2 | BAA04g11350 | A04 | 17283962 | C | T | upstream_gene_variant | MODIFIER | c.-3962C>T| |
S249 |
3 | BAA04g11350 | A04 | 17284115 | G | A | upstream_gene_variant | MODIFIER | c.-3809G>A| |
S266 |
4 | BAA04g11350 | A04 | 17287431 | G | A | upstream_gene_variant | MODIFIER | c.-493G>A| |
S211 S227 |
5 | BAA04g11350 | A04 | 17287942 | G | A | missense_variant | MODERATE | c.19G>A|p.Glu7Lys |
S166 S167 S236 S257 S262 |
6 | BAA04g11350 | A04 | 17287993 | C | T | synonymous_variant | LOW | c.70C>T|p.Leu24Leu |
S242 |
7 | BAA04g11350 | A04 | 17288203 | C | T | intron_variant | MODIFIER | c.153-31C>T| |
S207 |
8 | BAA04g11350 | A04 | 17289237 | G | A | intron_variant | MODIFIER | c.473-216G>A| |
S125 |
9 | BAA04g11350 | A04 | 17289265 | C | T | intron_variant | MODIFIER | c.473-188C>T| |
S293 |
10 | BAA04g11350 | A04 | 17290443 | G | A | intron_variant | MODIFIER | c.753+710G>A| |
S127 |
11 | BAA04g11350 | A04 | 17291355 | G | A | intron_variant | MODIFIER | c.754-1607G>A| |
S219 |
12 | BAA04g11350 | A04 | 17291664 | G | A | intron_variant | MODIFIER | c.754-1298G>A| |
S12 |
13 | BAA04g11350 | A04 | 17292299 | G | A | intron_variant | MODIFIER | c.754-663G>A| |
S264 |
14 | BAA04g11350 | A04 | 17293259 | G | A | missense_variant | MODERATE | c.983G>A|p.Gly328Glu |
S169 |
15 | BAA04g11350 | A04 | 17294882 | C | T | missense_variant&splice_region_variant | MODERATE | c.1109C>T|p.Ala370Val |
S182 |
16 | BAA04g11350 | A04 | 17295260 | G | A | downstream_gene_variant | MODIFIER | c.*125G>A| |
S261 |
17 | BAA04g11350 | A04 | 17296784 | G | A | downstream_gene_variant | MODIFIER | c.*1649G>A| |
S241 |