Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g33450 | A04 | 30504357 | A | C | downstream_gene_variant | MODIFIER | c.*4994T>G| |
S117 S195 S229 S251 S252 S31 S38 S66 |
2 | BAA04g33450 | A04 | 30504386 | G | A | downstream_gene_variant | MODIFIER | c.*4965C>T| |
S12 S187 S193 S201 S222 |
3 | BAA04g33450 | A04 | 30504408 | T | C | downstream_gene_variant | MODIFIER | c.*4943A>G| |
S105 S108 S120 S122 S143 S170 S188 S231 S242 S303 S308 |
4 | BAA04g33450 | A04 | 30504413 | G | A | downstream_gene_variant | MODIFIER | c.*4938C>T| |
S104 S173 S211 S298 S54 S63 |
5 | BAA04g33450 | A04 | 30504434 | G | A | downstream_gene_variant | MODIFIER | c.*4917C>T| |
S132 S164 S168 S169 S188 S190 S213 S235 S261 S280 S86 |
6 | BAA04g33450 | A04 | 30504445 | A | C | downstream_gene_variant | MODIFIER | c.*4906T>G| |
S104 S105 S260 S276 S291 S296 S57 S8 |
7 | BAA04g33450 | A04 | 30504459 | A | T | downstream_gene_variant | MODIFIER | c.*4892T>A| |
S132 S149 S164 S75 S86 |
8 | BAA04g33450 | A04 | 30504472 | T | G | downstream_gene_variant | MODIFIER | c.*4879A>C| |
S120 S151 S238 S241 S303 S85 |
9 | BAA04g33450 | A04 | 30504526 | G | A | downstream_gene_variant | MODIFIER | c.*4825C>T| |
S179 S225 S227 S243 S251 S271 S272 S276 S280 S32 S50 |
10 | BAA04g33450 | A04 | 30504552 | C | T | downstream_gene_variant | MODIFIER | c.*4799G>A| |
S100 S222 S228 S306 S83 S85 S94 |
11 | BAA04g33450 | A04 | 30506743 | C | T | downstream_gene_variant | MODIFIER | c.*2608G>A| |
S10 |
12 | BAA04g33450 | A04 | 30507562 | G | A | downstream_gene_variant | MODIFIER | c.*1789C>T| |
S150 |
13 | BAA04g33450 | A04 | 30509538 | C | T | missense_variant | MODERATE | c.1919G>A|p.Gly640Glu |
S296 |
14 | BAA04g33450 | A04 | 30510076 | C | T | synonymous_variant | LOW | c.1533G>A|p.Glu511Glu |
S100 |
15 | BAA04g33450 | A04 | 30510143 | G | A | missense_variant | MODERATE | c.1466C>T|p.Thr489Ile |
S162 |
16 | BAA04g33450 | A04 | 30510600 | G | A | intron_variant | MODIFIER | c.1123-28C>T| |
S274 |
17 | BAA04g33450 | A04 | 30511810 | C | T | missense_variant | MODERATE | c.257G>A|p.Gly86Glu |
S173 |
18 | BAA04g33450 | A04 | 30511859 | G | A | stop_gained | HIGH | c.208C>T|p.Gln70* |
S206 |
19 | BAA04g33450 | A04 | 30513134 | C | T | upstream_gene_variant | MODIFIER | c.-1001G>A| |
S81 S85 |
20 | BAA04g33450 | A04 | 30515959 | G | A | upstream_gene_variant | MODIFIER | c.-3826C>T| |
S274 |
21 | BAA04g33450 | A04 | 30516967 | C | T | upstream_gene_variant | MODIFIER | c.-4834G>A| |
S117 |