Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g40600 | A01 | 26889513 | G | A | synonymous_variant | LOW | c.4273C>T|p.Leu1425Leu |
S138 |
2 | BAA01g40600 | A01 | 26889820 | G | A | synonymous_variant | LOW | c.3966C>T|p.Asp1322Asp |
S139 |
3 | BAA01g40600 | A01 | 26891394 | C | T | missense_variant | MODERATE | c.2980G>A|p.Gly994Arg |
S186 |
4 | BAA01g40600 | A01 | 26891429 | C | T | missense_variant | MODERATE | c.2945G>A|p.Arg982His |
S50 |
5 | BAA01g40600 | A01 | 26891701 | C | T | synonymous_variant | LOW | c.2673G>A|p.Ala891Ala |
S259 |
6 | BAA01g40600 | A01 | 26891961 | C | T | missense_variant | MODERATE | c.2413G>A|p.Gly805Arg |
S279 |
7 | BAA01g40600 | A01 | 26891979 | C | T | missense_variant | MODERATE | c.2395G>A|p.Gly799Arg |
S48 |
8 | BAA01g40600 | A01 | 26892140 | G | A | synonymous_variant | LOW | c.2322C>T|p.Asp774Asp |
S185 |
9 | BAA01g40600 | A01 | 26892980 | G | A | missense_variant | MODERATE | c.2014C>T|p.Pro672Ser |
S67 |
10 | BAA01g40600 | A01 | 26893219 | C | T | missense_variant | MODERATE | c.1775G>A|p.Arg592Lys |
S206 S26 |
11 | BAA01g40600 | A01 | 26896405 | C | T | upstream_gene_variant | MODIFIER | c.-1412G>A| |
S59 |
12 | BAA01g40600 | A01 | 26896710 | A | T | upstream_gene_variant | MODIFIER | c.-1717T>A| |
S14 |
13 | BAA01g40600 | A01 | 26896849 | C | T | upstream_gene_variant | MODIFIER | c.-1856G>A| |
S68 |
14 | BAA01g40600 | A01 | 26897245 | C | T | upstream_gene_variant | MODIFIER | c.-2252G>A| |
S133 |
15 | BAA01g40600 | A01 | 26897413 | C | T | upstream_gene_variant | MODIFIER | c.-2420G>A| |
S242 |
16 | BAA01g40600 | A01 | 26897923 | G | A | upstream_gene_variant | MODIFIER | c.-2930C>T| |
S77 |