Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19820 | A10 | 18050019 | C | T | missense_variant | MODERATE | c.1700G>A|p.Gly567Glu |
S266 |
2 | BAA10g19820 | A10 | 18050224 | C | T | missense_variant | MODERATE | c.1495G>A|p.Glu499Lys |
S283 |
3 | BAA10g19820 | A10 | 18050447 | G | A | missense_variant | MODERATE | c.1360C>T|p.Leu454Phe |
S303 |
4 | BAA10g19820 | A10 | 18050677 | C | T | missense_variant | MODERATE | c.1211G>A|p.Gly404Glu |
S70 |
5 | BAA10g19820 | A10 | 18051179 | G | A | synonymous_variant | LOW | c.936C>T|p.Leu312Leu |
S234 |
6 | BAA10g19820 | A10 | 18052340 | C | T | splice_region_variant&synonymous_variant | LOW | c.708G>A|p.Lys236Lys |
S260 |
7 | BAA10g19820 | A10 | 18053566 | G | A | missense_variant | MODERATE | c.164C>T|p.Ala55Val |
S18 |