Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22180 | A01 | 11087454 | G | A | missense_variant | MODERATE | c.2795C>T|p.Ser932Phe |
S178 |
2 | BAA01g22180 | A01 | 11089690 | C | T | missense_variant | MODERATE | c.1879G>A|p.Gly627Ser |
S135 |
3 | BAA01g22180 | A01 | 11089838 | C | T | synonymous_variant | LOW | c.1803G>A|p.Lys601Lys |
S176 |
4 | BAA01g22180 | A01 | 11090482 | C | T | missense_variant | MODERATE | c.1508G>A|p.Arg503Lys |
S17 |
5 | BAA01g22180 | A01 | 11090799 | G | A | missense_variant | MODERATE | c.1373C>T|p.Thr458Ile |
S178 |
6 | BAA01g22180 | A01 | 11090809 | G | A | missense_variant | MODERATE | c.1363C>T|p.Leu455Phe |
S217 |
7 | BAA01g22180 | A01 | 11091287 | C | T | missense_variant | MODERATE | c.1090G>A|p.Ala364Thr |
S96 |
8 | BAA01g22180 | A01 | 11091670 | G | A | synonymous_variant | LOW | c.951C>T|p.Leu317Leu |
S238 |
9 | BAA01g22180 | A01 | 11092021 | G | A | intron_variant | MODIFIER | c.753+20C>T| |
S87 |
10 | BAA01g22180 | A01 | 11092259 | C | T | missense_variant | MODERATE | c.692G>A|p.Gly231Asp |
S143 |
11 | BAA01g22180 | A01 | 11092584 | G | A | missense_variant | MODERATE | c.565C>T|p.Pro189Ser |
S109 |
12 | BAA01g22180 | A01 | 11096564 | C | T | upstream_gene_variant | MODIFIER | c.-2782G>A| |
S198 |
13 | BAA01g22180 | A01 | 11096831 | C | T | upstream_gene_variant | MODIFIER | c.-3049G>A| |
S140 |
14 | BAA01g22180 | A01 | 11097074 | G | A | upstream_gene_variant | MODIFIER | c.-3292C>T| |
S244 |
15 | BAA01g22180 | A01 | 11098776 | C | T | upstream_gene_variant | MODIFIER | c.-4994G>A| |
S183 |