Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g10250 | A06 | 5170807 | G | A | missense_variant&splice_region_variant | MODERATE | c.1076C>T|p.Pro359Leu |
S233 |
2 | BAA06g10250 | A06 | 5171568 | C | T | splice_donor_variant&intron_variant | HIGH | c.721+1G>A| |
S245 |
3 | BAA06g10250 | A06 | 5172295 | C | T | synonymous_variant | LOW | c.381G>A|p.Gly127Gly |
S250 |
4 | BAA06g10250 | A06 | 5172571 | C | T | splice_region_variant&intron_variant | LOW | c.286+5G>A| |
S23 |
5 | BAA06g10250 | A06 | 5172578 | G | A | missense_variant&splice_region_variant | MODERATE | c.284C>T|p.Ser95Leu |
S54 |
6 | BAA06g10250 | A06 | 5172985 | G | A | synonymous_variant | LOW | c.132C>T|p.Val44Val |
S166 |
7 | BAA06g10250 | A06 | 5176808 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S225 S73 |
8 | BAA06g10250 | A06 | 5177256 | C | T | upstream_gene_variant | MODIFIER | c.-4140G>A| |
S13 |