Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41920 | A02 | 35006397 | C | T | missense_variant&splice_region_variant | MODERATE | c.85G>A|p.Gly29Ser |
S283 |
2 | BAA02g41920 | A02 | 35007983 | G | A | upstream_gene_variant | MODIFIER | c.-1345C>T| |
S136 |
3 | BAA02g41920 | A02 | 35008779 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S167 |
4 | BAA02g41920 | A02 | 35009121 | C | T | upstream_gene_variant | MODIFIER | c.-2483G>A| |
S128 |
5 | BAA02g41920 | A02 | 35009282 | C | T | upstream_gene_variant | MODIFIER | c.-2644G>A| |
S162 |
6 | BAA02g41920 | A02 | 35009406 | C | T | upstream_gene_variant | MODIFIER | c.-2768G>A| |
S170 |
7 | BAA02g41920 | A02 | 35009984 | C | T | upstream_gene_variant | MODIFIER | c.-3346G>A| |
S179 |
8 | BAA02g41920 | A02 | 35010124 | C | T | upstream_gene_variant | MODIFIER | c.-3486G>A| |
S170 |
9 | BAA02g41920 | A02 | 35010414 | C | T | upstream_gene_variant | MODIFIER | c.-3776G>A| |
S95 |