Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26590 | A09 | 17284648 | C | T | downstream_gene_variant | MODIFIER | c.*1914G>A| |
S67 |
2 | BAA09g26590 | A09 | 17284708 | C | T | downstream_gene_variant | MODIFIER | c.*1854G>A| |
S39 |
3 | BAA09g26590 | A09 | 17284903 | G | T | downstream_gene_variant | MODIFIER | c.*1659C>A| |
S132 S137 S215 S89 |
4 | BAA09g26590 | A09 | 17285057 | G | A | downstream_gene_variant | MODIFIER | c.*1505C>T| |
S151 S263 |
5 | BAA09g26590 | A09 | 17285135 | C | T | downstream_gene_variant | MODIFIER | c.*1427G>A| |
S150 |
6 | BAA09g26590 | A09 | 17285705 | G | A | downstream_gene_variant | MODIFIER | c.*857C>T| |
S249 |
7 | BAA09g26590 | A09 | 17286353 | C | T | downstream_gene_variant | MODIFIER | c.*209G>A| |
S5 |
8 | BAA09g26590 | A09 | 17286647 | G | A | missense_variant | MODERATE | c.1334C>T|p.Pro445Leu |
S152 |
9 | BAA09g26590 | A09 | 17287053 | C | T | intron_variant | MODIFIER | c.1135-207G>A| |
S230 |
10 | BAA09g26590 | A09 | 17287424 | C | T | intron_variant | MODIFIER | c.1134+235G>A| |
S247 |
11 | BAA09g26590 | A09 | 17288423 | C | T | intron_variant | MODIFIER | c.845-310G>A| |
S111 |
12 | BAA09g26590 | A09 | 17288479 | G | A | intron_variant | MODIFIER | c.845-366C>T| |
S122 |
13 | BAA09g26590 | A09 | 17288710 | C | T | intron_variant | MODIFIER | c.844+314G>A| |
S68 |
14 | BAA09g26590 | A09 | 17289059 | C | T | missense_variant | MODERATE | c.809G>A|p.Gly270Glu |
S133 |
15 | BAA09g26590 | A09 | 17289992 | G | A | upstream_gene_variant | MODIFIER | c.-125C>T| |
S217 |
16 | BAA09g26590 | A09 | 17291042 | C | T | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S104 S52 |
17 | BAA09g26590 | A09 | 17291173 | G | A | upstream_gene_variant | MODIFIER | c.-1306C>T| |
S162 |
18 | BAA09g26590 | A09 | 17291602 | C | T | upstream_gene_variant | MODIFIER | c.-1735G>A| |
S272 |