Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g21840 | A03 | 9908040 | C | T | downstream_gene_variant | MODIFIER | c.*2080G>A| |
S205 |
2 | BAA03g21840 | A03 | 9908093 | G | A | downstream_gene_variant | MODIFIER | c.*2027C>T| |
S14 |
3 | BAA03g21840 | A03 | 9909471 | C | T | downstream_gene_variant | MODIFIER | c.*649G>A| |
S107 S166 |
4 | BAA03g21840 | A03 | 9909784 | C | T | downstream_gene_variant | MODIFIER | c.*336G>A| |
S279 |
5 | BAA03g21840 | A03 | 9910429 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1144-1G>A| |
S153 |
6 | BAA03g21840 | A03 | 9911546 | G | A | missense_variant | MODERATE | c.737C>T|p.Thr246Met |
S17 |
7 | BAA03g21840 | A03 | 9911613 | G | A | synonymous_variant | LOW | c.670C>T|p.Leu224Leu |
S192 |
8 | BAA03g21840 | A03 | 9911792 | G | A | missense_variant | MODERATE | c.491C>T|p.Pro164Leu |
S138 |
9 | BAA03g21840 | A03 | 9911849 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S182 |
10 | BAA03g21840 | A03 | 9912539 | C | T | upstream_gene_variant | MODIFIER | c.-257G>A| |
S257 |
11 | BAA03g21840 | A03 | 9913188 | T | A | upstream_gene_variant | MODIFIER | c.-906A>T| |
S116 |
12 | BAA03g21840 | A03 | 9913555 | G | A | upstream_gene_variant | MODIFIER | c.-1273C>T| |
S136 |
13 | BAA03g21840 | A03 | 9914696 | C | T | upstream_gene_variant | MODIFIER | c.-2414G>A| |
S158 |
14 | BAA03g21840 | A03 | 9915325 | C | T | upstream_gene_variant | MODIFIER | c.-3043G>A| |
S139 |
15 | BAA03g21840 | A03 | 9916108 | G | A | upstream_gene_variant | MODIFIER | c.-3826C>T| |
S294 |