Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g24230 | A06 | 16086750 | G | A | missense_variant | MODERATE | c.5116C>T|p.Leu1706Phe |
S255 |
2 | BAA06g24230 | A06 | 16087053 | G | A | missense_variant | MODERATE | c.4903C>T|p.Leu1635Phe |
S268 |
3 | BAA06g24230 | A06 | 16087063 | C | T | synonymous_variant | LOW | c.4893G>A|p.Thr1631Thr |
S205 |
4 | BAA06g24230 | A06 | 16087552 | C | T | synonymous_variant | LOW | c.4578G>A|p.Glu1526Glu |
S148 S210 S30 S31 |
5 | BAA06g24230 | A06 | 16087719 | G | A | synonymous_variant | LOW | c.4524C>T|p.Pro1508Pro |
S12 |
6 | BAA06g24230 | A06 | 16088111 | C | T | synonymous_variant | LOW | c.4218G>A|p.Val1406Val |
S221 |
7 | BAA06g24230 | A06 | 16088315 | C | T | missense_variant | MODERATE | c.4084G>A|p.Val1362Ile |
S212 |
8 | BAA06g24230 | A06 | 16089281 | G | A | missense_variant | MODERATE | c.3526C>T|p.Leu1176Phe |
S308 |
9 | BAA06g24230 | A06 | 16090129 | C | T | intron_variant | MODIFIER | c.3102+115G>A| |
S167 |
10 | BAA06g24230 | A06 | 16090461 | G | A | missense_variant | MODERATE | c.2885C>T|p.Ser962Phe |
S44 |
11 | BAA06g24230 | A06 | 16090509 | G | A | missense_variant | MODERATE | c.2837C>T|p.Ser946Phe |
S85 |
12 | BAA06g24230 | A06 | 16090843 | C | T | missense_variant | MODERATE | c.2647G>A|p.Asp883Asn |
S156 |
13 | BAA06g24230 | A06 | 16091561 | C | T | intron_variant | MODIFIER | c.2063+20G>A| |
S287 |
14 | BAA06g24230 | A06 | 16091769 | C | T | splice_region_variant&intron_variant | LOW | c.1879-4G>A| |
S245 |
15 | BAA06g24230 | A06 | 16091786 | C | T | intron_variant | MODIFIER | c.1879-21G>A| |
S279 |
16 | BAA06g24230 | A06 | 16092025 | G | A | synonymous_variant | LOW | c.1761C>T|p.Ile587Ile |
S294 |
17 | BAA06g24230 | A06 | 16092233 | C | T | intron_variant | MODIFIER | c.1573-20G>A| |
S79 S84 |
18 | BAA06g24230 | A06 | 16092411 | C | T | missense_variant | MODERATE | c.1513G>A|p.Ala505Thr |
S275 |
19 | BAA06g24230 | A06 | 16092478 | G | A | intron_variant | MODIFIER | c.1474-28C>T| |
S76 |
20 | BAA06g24230 | A06 | 16092670 | A | T | intron_variant | MODIFIER | c.1377-28T>A| |
S136 |
21 | BAA06g24230 | A06 | 16092841 | G | A | intron_variant | MODIFIER | c.1288-18C>T| |
S89 |
22 | BAA06g24230 | A06 | 16092862 | G | A | intron_variant | MODIFIER | c.1288-39C>T| |
S69 |
23 | BAA06g24230 | A06 | 16092896 | G | A | intron_variant | MODIFIER | c.1287+18C>T| |
S201 |
24 | BAA06g24230 | A06 | 16093989 | C | T | synonymous_variant | LOW | c.963G>A|p.Lys321Lys |
S189 |
25 | BAA06g24230 | A06 | 16094742 | C | T | splice_region_variant&intron_variant | LOW | c.717+5G>A| |
S164 |