Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32670 | A01 | 21623742 | C | T | missense_variant | MODERATE | c.325G>A|p.Glu109Lys |
S242 |
2 | BAA01g32670 | A01 | 21624327 | G | A | intron_variant | MODIFIER | c.316-576C>T| |
S138 S296 |
3 | BAA01g32670 | A01 | 21625422 | C | T | intron_variant | MODIFIER | c.316-1671G>A| |
S208 S219 |
4 | BAA01g32670 | A01 | 21625594 | G | A | intron_variant | MODIFIER | c.316-1843C>T| |
S1 |
5 | BAA01g32670 | A01 | 21626400 | C | T | intron_variant | MODIFIER | c.316-2649G>A| |
S130 |
6 | BAA01g32670 | A01 | 21627935 | G | A | intron_variant | MODIFIER | c.315+2046C>T| |
S5 |
7 | BAA01g32670 | A01 | 21628561 | G | A | intron_variant | MODIFIER | c.315+1420C>T| |
S110 |
8 | BAA01g32670 | A01 | 21629414 | G | A | intron_variant | MODIFIER | c.315+567C>T| |
S270 |
9 | BAA01g32670 | A01 | 21629495 | G | A | intron_variant | MODIFIER | c.315+486C>T| |
S262 |
10 | BAA01g32670 | A01 | 21629782 | C | T | intron_variant | MODIFIER | c.315+199G>A| |
S200 |
11 | BAA01g32670 | A01 | 21629949 | G | A | intron_variant | MODIFIER | c.315+32C>T| |
S144 |
12 | BAA01g32670 | A01 | 21630165 | C | T | intron_variant | MODIFIER | c.268+73G>A| |
S117 |
13 | BAA01g32670 | A01 | 21630279 | G | A | missense_variant | MODERATE | c.227C>T|p.Pro76Leu |
S259 |
14 | BAA01g32670 | A01 | 21630282 | G | A | missense_variant | MODERATE | c.224C>T|p.Ser75Phe |
S139 |
15 | BAA01g32670 | A01 | 21630663 | C | T | upstream_gene_variant | MODIFIER | c.-158G>A| |
S269 |
16 | BAA01g32670 | A01 | 21630856 | C | T | upstream_gene_variant | MODIFIER | c.-351G>A| |
S51 |
17 | BAA01g32670 | A01 | 21633413 | G | A | upstream_gene_variant | MODIFIER | c.-2908C>T| |
S305 |
18 | BAA01g32670 | A01 | 21634291 | C | T | upstream_gene_variant | MODIFIER | c.-3786G>A| |
S98 |
19 | BAA01g32670 | A01 | 21634331 | C | T | upstream_gene_variant | MODIFIER | c.-3826G>A| |
S192 |
20 | BAA01g32670 | A01 | 21634369 | C | T | upstream_gene_variant | MODIFIER | c.-3864G>A| |
S216 |