Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32700 | A01 | 21661248 | C | T | upstream_gene_variant | MODIFIER | c.-3154C>T| |
S205 |
2 | BAA01g32700 | A01 | 21661256 | C | T | upstream_gene_variant | MODIFIER | c.-3146C>T| |
S28 |
3 | BAA01g32700 | A01 | 21661463 | G | A | upstream_gene_variant | MODIFIER | c.-2939G>A| |
S221 |
4 | BAA01g32700 | A01 | 21661975 | G | A | upstream_gene_variant | MODIFIER | c.-2427G>A| |
S308 |
5 | BAA01g32700 | A01 | 21662921 | G | A | upstream_gene_variant | MODIFIER | c.-1481G>A| |
S176 |
6 | BAA01g32700 | A01 | 21663461 | C | T | upstream_gene_variant | MODIFIER | c.-941C>T| |
S64 |
7 | BAA01g32700 | A01 | 21664466 | G | A | missense_variant | MODERATE | c.65G>A|p.Arg22His |
S129 |
8 | BAA01g32700 | A01 | 21665451 | G | A | synonymous_variant | LOW | c.1050G>A|p.Ser350Ser |
S197 |
9 | BAA01g32700 | A01 | 21665557 | G | A | missense_variant | MODERATE | c.1156G>A|p.Gly386Arg |
S263 |
10 | BAA01g32700 | A01 | 21665570 | C | T | missense_variant | MODERATE | c.1169C>T|p.Ser390Leu |
S120 |
11 | BAA01g32700 | A01 | 21665616 | A | G | intron_variant | MODIFIER | c.1192+23A>G| |
S128 |
12 | BAA01g32700 | A01 | 21666276 | C | T | intron_variant | MODIFIER | c.1193-181C>T| |
S251 |
13 | BAA01g32700 | A01 | 21666464 | C | T | synonymous_variant | LOW | c.1200C>T|p.Val400Val |
S39 |
14 | BAA01g32700 | A01 | 21667633 | G | A | intron_variant | MODIFIER | c.1659+710G>A| |
S292 |
15 | BAA01g32700 | A01 | 21667853 | C | T | intron_variant | MODIFIER | c.1660-547C>T| |
S82 S92 |
16 | BAA01g32700 | A01 | 21669110 | C | T | synonymous_variant | LOW | c.2115C>T|p.Ile705Ile |
S18 |
17 | BAA01g32700 | A01 | 21673423 | G | A | downstream_gene_variant | MODIFIER | c.*3662G>A| |
S173 |
18 | BAA01g32700 | A01 | 21674485 | C | T | downstream_gene_variant | MODIFIER | c.*4724C>T| |
S40 S49 |