Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16640 | A01 | 8096852 | C | T | synonymous_variant | LOW | c.2049G>A|p.Gly683Gly |
S179 |
2 | BAA01g16640 | A01 | 8097364 | C | T | synonymous_variant | LOW | c.1815G>A|p.Arg605Arg |
S289 S290 |
3 | BAA01g16640 | A01 | 8097489 | G | A | stop_gained | HIGH | c.1690C>T|p.Arg564* |
S115 |
4 | BAA01g16640 | A01 | 8099194 | C | T | splice_region_variant&intron_variant | LOW | c.1062+6G>A| |
S120 |
5 | BAA01g16640 | A01 | 8099319 | G | A | missense_variant | MODERATE | c.943C>T|p.Pro315Ser |
S105 S106 |
6 | BAA01g16640 | A01 | 8099323 | G | A | synonymous_variant | LOW | c.939C>T|p.Leu313Leu |
S259 |
7 | BAA01g16640 | A01 | 8102195 | G | A | missense_variant | MODERATE | c.32C>T|p.Pro11Leu |
S191 |
8 | BAA01g16640 | A01 | 8102534 | G | A | upstream_gene_variant | MODIFIER | c.-308C>T| |
S5 |
9 | BAA01g16640 | A01 | 8102992 | C | T | upstream_gene_variant | MODIFIER | c.-766G>A| |
S53 |
10 | BAA01g16640 | A01 | 8105560 | C | T | upstream_gene_variant | MODIFIER | c.-3334G>A| |
S200 |