Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41590 | A03 | 19512726 | G | A | downstream_gene_variant | MODIFIER | c.*4376C>T| |
S164 |
2 | BAA03g41590 | A03 | 19513471 | G | A | downstream_gene_variant | MODIFIER | c.*3631C>T| |
S146 |
3 | BAA03g41590 | A03 | 19513816 | C | T | downstream_gene_variant | MODIFIER | c.*3286G>A| |
S183 S198 |
4 | BAA03g41590 | A03 | 19515291 | C | T | downstream_gene_variant | MODIFIER | c.*1811G>A| |
S192 |
5 | BAA03g41590 | A03 | 19515294 | C | T | downstream_gene_variant | MODIFIER | c.*1808G>A| |
S15 |
6 | BAA03g41590 | A03 | 19515400 | C | T | downstream_gene_variant | MODIFIER | c.*1702G>A| |
S180 |
7 | BAA03g41590 | A03 | 19515562 | G | A | downstream_gene_variant | MODIFIER | c.*1540C>T| |
S167 |
8 | BAA03g41590 | A03 | 19516348 | G | A | downstream_gene_variant | MODIFIER | c.*754C>T| |
S20 |
9 | BAA03g41590 | A03 | 19517379 | G | A | intron_variant | MODIFIER | c.1634-180C>T| |
S74 |
10 | BAA03g41590 | A03 | 19517529 | G | A | intron_variant | MODIFIER | c.1633+169C>T| |
S94 |
11 | BAA03g41590 | A03 | 19517720 | G | A | synonymous_variant | LOW | c.1611C>T|p.Ser537Ser |
S168 |
12 | BAA03g41590 | A03 | 19517871 | G | A | missense_variant | MODERATE | c.1460C>T|p.Ala487Val |
S226 |
13 | BAA03g41590 | A03 | 19518189 | C | T | missense_variant | MODERATE | c.1142G>A|p.Gly381Glu |
S8 |
14 | BAA03g41590 | A03 | 19519135 | C | T | missense_variant | MODERATE | c.535G>A|p.Gly179Ser |
S293 |
15 | BAA03g41590 | A03 | 19519143 | C | T | missense_variant | MODERATE | c.527G>A|p.Gly176Glu |
S184 |
16 | BAA03g41590 | A03 | 19520569 | C | T | intron_variant | MODIFIER | c.437+573G>A| |
S211 S227 |
17 | BAA03g41590 | A03 | 19520874 | C | T | intron_variant | MODIFIER | c.437+268G>A| |
S192 |
18 | BAA03g41590 | A03 | 19522052 | C | T | upstream_gene_variant | MODIFIER | c.-348G>A| |
S79 S91 |