Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41150 | A01 | 27374168 | G | A | downstream_gene_variant | MODIFIER | c.*3842C>T| |
S185 |
2 | BAA01g41150 | A01 | 27374731 | C | T | downstream_gene_variant | MODIFIER | c.*3279G>A| |
S168 |
3 | BAA01g41150 | A01 | 27376275 | C | T | downstream_gene_variant | MODIFIER | c.*1735G>A| |
S103 |
4 | BAA01g41150 | A01 | 27377255 | C | T | downstream_gene_variant | MODIFIER | c.*755G>A| |
S166 S167 |
5 | BAA01g41150 | A01 | 27378307 | G | A | synonymous_variant | LOW | c.186C>T|p.Leu62Leu |
S77 S82 |
6 | BAA01g41150 | A01 | 27378376 | G | A | synonymous_variant | LOW | c.117C>T|p.Arg39Arg |
S20 |
7 | BAA01g41150 | A01 | 27378414 | C | T | missense_variant | MODERATE | c.79G>A|p.Glu27Lys |
S255 |
8 | BAA01g41150 | A01 | 27379046 | G | A | upstream_gene_variant | MODIFIER | c.-554C>T| |
S306 S308 |
9 | BAA01g41150 | A01 | 27379276 | C | T | upstream_gene_variant | MODIFIER | c.-784G>A| |
S170 S247 |
10 | BAA01g41150 | A01 | 27379667 | C | T | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S12 |
11 | BAA01g41150 | A01 | 27381375 | G | A | upstream_gene_variant | MODIFIER | c.-2883C>T| |
S20 |
12 | BAA01g41150 | A01 | 27382590 | C | T | upstream_gene_variant | MODIFIER | c.-4098G>A| |
S56 |
13 | BAA01g41150 | A01 | 27382851 | G | C | upstream_gene_variant | MODIFIER | c.-4359C>G| |
S264 |