Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g07700 | A06 | 4033201 | G | A | missense_variant | MODERATE | c.136G>A|p.Gly46Arg |
S176 |
2 | BAA06g07700 | A06 | 4033946 | C | T | missense_variant | MODERATE | c.605C>T|p.Ser202Phe |
S84 S93 |
3 | BAA06g07700 | A06 | 4033971 | C | T | synonymous_variant | LOW | c.630C>T|p.Ala210Ala |
S245 |
4 | BAA06g07700 | A06 | 4033995 | G | A | stop_gained | HIGH | c.654G>A|p.Trp218* |
S235 |
5 | BAA06g07700 | A06 | 4034100 | G | A | synonymous_variant | LOW | c.759G>A|p.Gln253Gln |
S176 |
6 | BAA06g07700 | A06 | 4034128 | G | A | missense_variant | MODERATE | c.787G>A|p.Gly263Ser |
S159 S299 |
7 | BAA06g07700 | A06 | 4034369 | C | T | missense_variant | MODERATE | c.916C>T|p.Pro306Ser |
S270 |
8 | BAA06g07700 | A06 | 4038939 | C | T | downstream_gene_variant | MODIFIER | c.*4565C>T| |
S157 |