Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04230 | A01 | 1897714 | C | T | synonymous_variant | LOW | c.3561G>A|p.Glu1187Glu |
S128 |
2 | BAA01g04230 | A01 | 1897724 | G | A | missense_variant | MODERATE | c.3551C>T|p.Ser1184Leu |
S276 |
3 | BAA01g04230 | A01 | 1897930 | C | T | stop_gained | HIGH | c.3432G>A|p.Trp1144* |
S134 |
4 | BAA01g04230 | A01 | 1898481 | C | T | synonymous_variant | LOW | c.3147G>A|p.Gln1049Gln |
S158 |
5 | BAA01g04230 | A01 | 1900446 | C | T | missense_variant | MODERATE | c.1732G>A|p.Glu578Lys |
S58 |
6 | BAA01g04230 | A01 | 1900532 | G | A | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S263 |
7 | BAA01g04230 | A01 | 1900608 | C | T | missense_variant | MODERATE | c.1570G>A|p.Glu524Lys |
S36 |
8 | BAA01g04230 | A01 | 1901051 | G | A | missense_variant | MODERATE | c.1127C>T|p.Ala376Val |
S95 |
9 | BAA01g04230 | A01 | 1901857 | G | A | missense_variant | MODERATE | c.593C>T|p.Ala198Val |
S201 |
10 | BAA01g04230 | A01 | 1902115 | C | T | missense_variant | MODERATE | c.335G>A|p.Arg112Lys |
S38 |
11 | BAA01g04230 | A01 | 1902308 | G | A | missense_variant | MODERATE | c.142C>T|p.Pro48Ser |
S56 |
12 | BAA01g04230 | A01 | 1902660 | G | A | upstream_gene_variant | MODIFIER | c.-211C>T| |
S161 |
13 | BAA01g04230 | A01 | 1903010 | C | T | upstream_gene_variant | MODIFIER | c.-561G>A| |
S299 |
14 | BAA01g04230 | A01 | 1903639 | G | A | upstream_gene_variant | MODIFIER | c.-1190C>T| |
S85 |
15 | BAA01g04230 | A01 | 1903990 | G | A | upstream_gene_variant | MODIFIER | c.-1541C>T| |
S174 S241 S265 S27 |
16 | BAA01g04230 | A01 | 1905906 | G | A | upstream_gene_variant | MODIFIER | c.-3457C>T| |
S296 |
17 | BAA01g04230 | A01 | 1906420 | C | T | upstream_gene_variant | MODIFIER | c.-3971G>A| |
S99 |