Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g28690 | A01 | 17983142 | G | A | synonymous_variant | LOW | c.1227C>T|p.Ala409Ala |
S105 S106 |
2 | BAA01g28690 | A01 | 17985082 | C | T | intron_variant | MODIFIER | c.1167-1880G>A| |
S272 |
3 | BAA01g28690 | A01 | 17985726 | C | T | intron_variant | MODIFIER | c.1166+1845G>A| |
S282 |
4 | BAA01g28690 | A01 | 17985999 | C | T | intron_variant | MODIFIER | c.1166+1572G>A| |
S28 |
5 | BAA01g28690 | A01 | 17986180 | G | A | intron_variant | MODIFIER | c.1166+1391C>T| |
S85 |
6 | BAA01g28690 | A01 | 17987006 | C | T | intron_variant | MODIFIER | c.1166+565G>A| |
S28 |
7 | BAA01g28690 | A01 | 17987009 | G | A | intron_variant | MODIFIER | c.1166+562C>T| |
S15 S3 |
8 | BAA01g28690 | A01 | 17987095 | A | G | intron_variant | MODIFIER | c.1166+476T>C| |
S299 |
9 | BAA01g28690 | A01 | 17987739 | C | T | missense_variant | MODERATE | c.1079G>A|p.Cys360Tyr |
S200 |
10 | BAA01g28690 | A01 | 17987750 | G | A | synonymous_variant | LOW | c.1068C>T|p.Phe356Phe |
S298 |
11 | BAA01g28690 | A01 | 17987802 | C | T | missense_variant | MODERATE | c.1016G>A|p.Arg339Lys |
S172 S217 |
12 | BAA01g28690 | A01 | 17988068 | C | T | intron_variant | MODIFIER | c.884-48G>A| |
S155 S211 |
13 | BAA01g28690 | A01 | 17988412 | G | A | intron_variant | MODIFIER | c.884-392C>T| |
S217 |
14 | BAA01g28690 | A01 | 17989155 | G | A | intron_variant | MODIFIER | c.883+1002C>T| |
S72 S78 |
15 | BAA01g28690 | A01 | 17989276 | C | T | intron_variant | MODIFIER | c.883+881G>A| |
S48 |
16 | BAA01g28690 | A01 | 17989419 | G | A | intron_variant | MODIFIER | c.883+738C>T| |
S74 |
17 | BAA01g28690 | A01 | 17989490 | C | T | intron_variant | MODIFIER | c.883+667G>A| |
S276 |
18 | BAA01g28690 | A01 | 17989620 | C | T | intron_variant | MODIFIER | c.883+537G>A| |
S18 |
19 | BAA01g28690 | A01 | 17990110 | C | T | intron_variant | MODIFIER | c.883+47G>A| |
S295 |
20 | BAA01g28690 | A01 | 17990694 | G | A | intron_variant | MODIFIER | c.685-339C>T| |
S308 |
21 | BAA01g28690 | A01 | 17990805 | G | A | intron_variant | MODIFIER | c.685-450C>T| |
S265 |
22 | BAA01g28690 | A01 | 17991066 | G | A | intron_variant | MODIFIER | c.685-711C>T| |
S129 |
23 | BAA01g28690 | A01 | 17991779 | A | T | intron_variant | MODIFIER | c.684+469T>A| |
S209 |
24 | BAA01g28690 | A01 | 17991968 | G | A | intron_variant | MODIFIER | c.684+280C>T| |
S236 |
25 | BAA01g28690 | A01 | 17992276 | C | T | missense_variant | MODERATE | c.656G>A|p.Gly219Glu |
S223 |