Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19510 | A03 | 8645855 | G | A | synonymous_variant | LOW | c.84G>A|p.Arg28Arg |
S168 |
2 | BAA03g19510 | A03 | 8647997 | C | T | missense_variant | MODERATE | c.959C>T|p.Pro320Leu |
S48 |
3 | BAA03g19510 | A03 | 8648970 | C | T | synonymous_variant | LOW | c.1318C>T|p.Leu440Leu |
S38 |
4 | BAA03g19510 | A03 | 8649163 | C | A | intron_variant | MODIFIER | c.1357-85C>A| |
S115 |
5 | BAA03g19510 | A03 | 8649530 | C | T | missense_variant | MODERATE | c.1486C>T|p.Leu496Phe |
S92 |
6 | BAA03g19510 | A03 | 8649577 | C | T | synonymous_variant | LOW | c.1533C>T|p.Ser511Ser |
S173 |
7 | BAA03g19510 | A03 | 8650537 | T | C | intron_variant | MODIFIER | c.1576-57T>C| |
S69 |
8 | BAA03g19510 | A03 | 8650855 | C | T | missense_variant | MODERATE | c.1658C>T|p.Ala553Val |
S61 |
9 | BAA03g19510 | A03 | 8651458 | C | T | missense_variant | MODERATE | c.1882C>T|p.Leu628Phe |
S302 |
10 | BAA03g19510 | A03 | 8652386 | C | T | intron_variant | MODIFIER | c.2366-10C>T| |
S216 |
11 | BAA03g19510 | A03 | 8652595 | G | A | synonymous_variant | LOW | c.2493G>A|p.Ser831Ser |
S37 |
12 | BAA03g19510 | A03 | 8653552 | G | A | intron_variant | MODIFIER | c.3051+18G>A| |
S265 |
13 | BAA03g19510 | A03 | 8654385 | G | A | splice_region_variant&intron_variant | LOW | c.3486+5G>A| |
S169 |
14 | BAA03g19510 | A03 | 8654969 | C | T | intron_variant | MODIFIER | c.3786+23C>T| |
S250 |
15 | BAA03g19510 | A03 | 8655682 | C | T | intron_variant | MODIFIER | c.4082-32C>T| |
S121 |
16 | BAA03g19510 | A03 | 8659040 | G | A | missense_variant | MODERATE | c.5614G>A|p.Asp1872Asn |
S162 |
17 | BAA03g19510 | A03 | 8659253 | C | T | missense_variant | MODERATE | c.5827C>T|p.His1943Tyr |
S62 |