Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01600 | A08 | 1165047 | C | T | downstream_gene_variant | MODIFIER | c.*4724G>A| |
S67 |
2 | BAA08g01600 | A08 | 1171489 | C | T | intron_variant | MODIFIER | c.833+108G>A| |
S67 |
3 | BAA08g01600 | A08 | 1172055 | G | A | synonymous_variant | LOW | c.375C>T|p.Pro125Pro |
S125 |
4 | BAA08g01600 | A08 | 1172299 | G | A | missense_variant | MODERATE | c.131C>T|p.Thr44Ile |
S92 |
5 | BAA08g01600 | A08 | 1174329 | C | T | upstream_gene_variant | MODIFIER | c.-1900G>A| |
S245 |
6 | BAA08g01600 | A08 | 1174686 | C | T | upstream_gene_variant | MODIFIER | c.-2257G>A| |
S163 |
7 | BAA08g01600 | A08 | 1174752 | C | T | upstream_gene_variant | MODIFIER | c.-2323G>A| |
S275 |
8 | BAA08g01600 | A08 | 1175427 | G | A | upstream_gene_variant | MODIFIER | c.-2998C>T| |
S266 |
9 | BAA08g01600 | A08 | 1175428 | G | A | upstream_gene_variant | MODIFIER | c.-2999C>T| |
S274 |
10 | BAA08g01600 | A08 | 1175852 | G | A | upstream_gene_variant | MODIFIER | c.-3423C>T| |
S174 |
11 | BAA08g01600 | A08 | 1176645 | G | A | upstream_gene_variant | MODIFIER | c.-4216C>T| |
S273 |