Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g26790 | A03 | 12326360 | C | T | missense_variant | MODERATE | c.6712G>A|p.Asp2238Asn |
S1 S161 S244 S289 S290 S90 |
2 | BAA03g26790 | A03 | 12326949 | G | A | missense_variant | MODERATE | c.6644C>T|p.Ala2215Val |
S25 |
3 | BAA03g26790 | A03 | 12328020 | C | T | splice_region_variant&intron_variant | LOW | c.6201+5G>A| |
S19 |
4 | BAA03g26790 | A03 | 12328268 | G | A | intron_variant | MODIFIER | c.5973-15C>T| |
S17 |
5 | BAA03g26790 | A03 | 12331140 | G | A | intron_variant | MODIFIER | c.4240-23C>T| |
S5 |
6 | BAA03g26790 | A03 | 12331240 | C | T | missense_variant | MODERATE | c.4228G>A|p.Val1410Ile |
S121 |
7 | BAA03g26790 | A03 | 12331496 | C | T | intron_variant | MODIFIER | c.4149-177G>A| |
S45 |
8 | BAA03g26790 | A03 | 12331927 | C | T | intron_variant | MODIFIER | c.4148+92G>A| |
S53 |
9 | BAA03g26790 | A03 | 12332093 | C | T | synonymous_variant | LOW | c.4074G>A|p.Gln1358Gln |
S188 S298 |
10 | BAA03g26790 | A03 | 12332410 | G | A | missense_variant | MODERATE | c.3833C>T|p.Ser1278Phe |
S81 |
11 | BAA03g26790 | A03 | 12333108 | C | T | missense_variant | MODERATE | c.3229G>A|p.Val1077Ile |
S108 |
12 | BAA03g26790 | A03 | 12333764 | G | A | missense_variant | MODERATE | c.2893C>T|p.Leu965Phe |
S186 |
13 | BAA03g26790 | A03 | 12333837 | G | A | synonymous_variant | LOW | c.2820C>T|p.Ile940Ile |
S107 |
14 | BAA03g26790 | A03 | 12334057 | G | A | missense_variant | MODERATE | c.2729C>T|p.Ala910Val |
S142 |
15 | BAA03g26790 | A03 | 12334831 | C | T | intron_variant | MODIFIER | c.2500-195G>A| |
S156 |
16 | BAA03g26790 | A03 | 12334979 | G | A | intron_variant | MODIFIER | c.2499+74C>T| |
S160 |
17 | BAA03g26790 | A03 | 12335286 | C | T | missense_variant | MODERATE | c.2363G>A|p.Gly788Glu |
S194 |
18 | BAA03g26790 | A03 | 12337443 | C | T | intron_variant | MODIFIER | c.1557+64G>A| |
S255 |
19 | BAA03g26790 | A03 | 12337455 | G | A | intron_variant | MODIFIER | c.1557+52C>T| |
S262 |
20 | BAA03g26790 | A03 | 12337850 | G | A | missense_variant | MODERATE | c.1306C>T|p.Arg436Trp |
S286 |
21 | BAA03g26790 | A03 | 12338777 | G | A | synonymous_variant | LOW | c.864C>T|p.Leu288Leu |
S83 S88 |
22 | BAA03g26790 | A03 | 12338867 | G | A | synonymous_variant | LOW | c.774C>T|p.Leu258Leu |
S133 |
23 | BAA03g26790 | A03 | 12339837 | C | T | missense_variant | MODERATE | c.514G>A|p.Val172Ile |
S273 |
24 | BAA03g26790 | A03 | 12339941 | C | T | missense_variant | MODERATE | c.410G>A|p.Ser137Asn |
S207 |
25 | BAA03g26790 | A03 | 12340108 | G | A | synonymous_variant | LOW | c.243C>T|p.Asn81Asn |
S118 |