Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g37690 | A05 | 37018953 | C | T | missense_variant | MODERATE | c.269C>T|p.Ala90Val |
S10 |
2 | BAA05g37690 | A05 | 37020667 | G | A | synonymous_variant | LOW | c.1053G>A|p.Leu351Leu |
S291 |
3 | BAA05g37690 | A05 | 37021563 | G | A | missense_variant | MODERATE | c.1484G>A|p.Arg495Lys |
S138 |
4 | BAA05g37690 | A05 | 37022370 | G | A | synonymous_variant | LOW | c.1905G>A|p.Thr635Thr |
S155 |
5 | BAA05g37690 | A05 | 37023390 | C | T | stop_gained | HIGH | c.2473C>T|p.Gln825* |
S275 |
6 | BAA05g37690 | A05 | 37023547 | G | A | missense_variant | MODERATE | c.2630G>A|p.Arg877Gln |
S67 |
7 | BAA05g37690 | A05 | 37025013 | C | T | missense_variant | MODERATE | c.3491C>T|p.Ser1164Phe |
S233 |
8 | BAA05g37690 | A05 | 37025168 | G | A | missense_variant | MODERATE | c.3541G>A|p.Val1181Met |
S136 |
9 | BAA05g37690 | A05 | 37025214 | G | A | missense_variant | MODERATE | c.3587G>A|p.Arg1196Lys |
S18 |
10 | BAA05g37690 | A05 | 37025894 | G | A | downstream_gene_variant | MODIFIER | c.*47G>A| |
S232 |