Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26190 | A01 | 14533267 | C | T | intron_variant | MODIFIER | c.2068-53G>A| |
S17 |
2 | BAA01g26190 | A01 | 14533723 | C | T | intron_variant | MODIFIER | c.1816-33G>A| |
S277 |
3 | BAA01g26190 | A01 | 14534210 | C | T | synonymous_variant | LOW | c.1368G>A|p.Leu456Leu |
S260 |
4 | BAA01g26190 | A01 | 14534368 | G | A | stop_gained | HIGH | c.1210C>T|p.Arg404* |
S275 |
5 | BAA01g26190 | A01 | 14535139 | C | T | synonymous_variant | LOW | c.552G>A|p.Arg184Arg |
S273 |
6 | BAA01g26190 | A01 | 14535150 | C | T | missense_variant | MODERATE | c.541G>A|p.Val181Met |
S270 |
7 | BAA01g26190 | A01 | 14535336 | G | A | missense_variant | MODERATE | c.355C>T|p.Pro119Ser |
S169 |
8 | BAA01g26190 | A01 | 14535421 | G | T | missense_variant | MODERATE | c.270C>A|p.Asn90Lys |
S241 |
9 | BAA01g26190 | A01 | 14535458 | C | T | stop_gained | HIGH | c.233G>A|p.Trp78* |
S79 S84 |
10 | BAA01g26190 | A01 | 14535925 | G | A | upstream_gene_variant | MODIFIER | c.-8C>T| |
S299 |
11 | BAA01g26190 | A01 | 14536172 | C | T | upstream_gene_variant | MODIFIER | c.-255G>A| |
S270 |
12 | BAA01g26190 | A01 | 14536249 | G | A | upstream_gene_variant | MODIFIER | c.-332C>T| |
S238 |
13 | BAA01g26190 | A01 | 14536613 | C | T | upstream_gene_variant | MODIFIER | c.-696G>A| |
S35 |
14 | BAA01g26190 | A01 | 14537430 | G | A | upstream_gene_variant | MODIFIER | c.-1513C>T| |
S140 |
15 | BAA01g26190 | A01 | 14538880 | C | T | upstream_gene_variant | MODIFIER | c.-2963G>A| |
S82 S92 |
16 | BAA01g26190 | A01 | 14539228 | G | A | upstream_gene_variant | MODIFIER | c.-3311C>T| |
S198 |
17 | BAA01g26190 | A01 | 14539263 | G | A | upstream_gene_variant | MODIFIER | c.-3346C>T| |
S197 |
18 | BAA01g26190 | A01 | 14539576 | C | T | upstream_gene_variant | MODIFIER | c.-3659G>A| |
S223 |
19 | BAA01g26190 | A01 | 14540866 | G | A | upstream_gene_variant | MODIFIER | c.-4949C>T| |
S263 |