Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41170 | A09 | 47999800 | G | A | upstream_gene_variant | MODIFIER | c.-3680G>A| |
S202 |
2 | BAA09g41170 | A09 | 48001567 | G | A | upstream_gene_variant | MODIFIER | c.-1913G>A| |
S118 |
3 | BAA09g41170 | A09 | 48003299 | C | T | upstream_gene_variant | MODIFIER | c.-181C>T| |
S168 |
4 | BAA09g41170 | A09 | 48003714 | G | A | missense_variant | MODERATE | c.235G>A|p.Asp79Asn |
S164 |
5 | BAA09g41170 | A09 | 48004276 | C | T | intron_variant | MODIFIER | c.450+9C>T| |
S18 |
6 | BAA09g41170 | A09 | 48007551 | C | T | intron_variant | MODIFIER | c.589+3058C>T| |
S108 |
7 | BAA09g41170 | A09 | 48008192 | C | T | intron_variant | MODIFIER | c.590-3644C>T| |
S23 |
8 | BAA09g41170 | A09 | 48008628 | G | A | intron_variant | MODIFIER | c.590-3208G>A| |
S165 |
9 | BAA09g41170 | A09 | 48008702 | G | A | intron_variant | MODIFIER | c.590-3134G>A| |
S271 |
10 | BAA09g41170 | A09 | 48009291 | C | T | intron_variant | MODIFIER | c.590-2545C>T| |
S99 |
11 | BAA09g41170 | A09 | 48009319 | G | A | intron_variant | MODIFIER | c.590-2517G>A| |
S130 |
12 | BAA09g41170 | A09 | 48010502 | G | A | intron_variant | MODIFIER | c.590-1334G>A| |
S105 S106 |
13 | BAA09g41170 | A09 | 48010975 | G | A | intron_variant | MODIFIER | c.590-861G>A| |
S265 |
14 | BAA09g41170 | A09 | 48012066 | T | G | missense_variant | MODERATE | c.820T>G|p.Tyr274Asp |
S147 S247 S291 S49 S7 |
15 | BAA09g41170 | A09 | 48012125 | G | A | intron_variant | MODIFIER | c.829-32G>A| |
S71 |
16 | BAA09g41170 | A09 | 48013893 | G | A | downstream_gene_variant | MODIFIER | c.*1578G>A| |
S172 S217 |
17 | BAA09g41170 | A09 | 48015798 | G | A | downstream_gene_variant | MODIFIER | c.*3483G>A| |
S91 |