Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g11900 | A06 | 6017894 | G | A | missense_variant | MODERATE | c.2326C>T|p.Pro776Ser |
S123 |
2 | BAA06g11900 | A06 | 6018019 | G | A | missense_variant | MODERATE | c.2201C>T|p.Ser734Phe |
S234 |
3 | BAA06g11900 | A06 | 6019118 | G | A | synonymous_variant | LOW | c.1761C>T|p.Leu587Leu |
S38 |
4 | BAA06g11900 | A06 | 6019681 | C | T | missense_variant | MODERATE | c.1457G>A|p.Gly486Glu |
S296 |
5 | BAA06g11900 | A06 | 6020111 | G | A | missense_variant | MODERATE | c.1027C>T|p.Pro343Ser |
S139 |
6 | BAA06g11900 | A06 | 6020957 | C | T | missense_variant | MODERATE | c.283G>A|p.Val95Ile |
S172 S217 |
7 | BAA06g11900 | A06 | 6021485 | C | T | upstream_gene_variant | MODIFIER | c.-246G>A| |
S170 |
8 | BAA06g11900 | A06 | 6021943 | G | A | upstream_gene_variant | MODIFIER | c.-704C>T| |
S153 |
9 | BAA06g11900 | A06 | 6022123 | C | T | upstream_gene_variant | MODIFIER | c.-884G>A| |
S195 |