Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g50120 | A03 | 24179945 | C | T | missense_variant | MODERATE | c.1807G>A|p.Asp603Asn |
S241 S39 |
2 | BAA03g50120 | A03 | 24180099 | G | A | synonymous_variant | LOW | c.1653C>T|p.Asn551Asn |
S190 |
3 | BAA03g50120 | A03 | 24180358 | C | T | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S122 |
4 | BAA03g50120 | A03 | 24180390 | C | T | stop_gained | HIGH | c.1362G>A|p.Trp454* |
S276 |
5 | BAA03g50120 | A03 | 24180468 | C | T | stop_gained | HIGH | c.1284G>A|p.Trp428* |
S179 |
6 | BAA03g50120 | A03 | 24180754 | C | T | missense_variant | MODERATE | c.998G>A|p.Gly333Glu |
S266 |
7 | BAA03g50120 | A03 | 24181267 | C | T | missense_variant | MODERATE | c.485G>A|p.Gly162Asp |
S216 |
8 | BAA03g50120 | A03 | 24181488 | G | A | synonymous_variant | LOW | c.264C>T|p.Leu88Leu |
S138 |
9 | BAA03g50120 | A03 | 24181559 | C | T | missense_variant | MODERATE | c.193G>A|p.Asp65Asn |
S105 S106 |
10 | BAA03g50120 | A03 | 24181719 | G | A | synonymous_variant | LOW | c.33C>T|p.Leu11Leu |
S287 |
11 | BAA03g50120 | A03 | 24181938 | C | T | upstream_gene_variant | MODIFIER | c.-187G>A| |
S44 |
12 | BAA03g50120 | A03 | 24182293 | G | A | upstream_gene_variant | MODIFIER | c.-542C>T| |
S136 |
13 | BAA03g50120 | A03 | 24182964 | G | A | upstream_gene_variant | MODIFIER | c.-1213C>T| |
S191 |
14 | BAA03g50120 | A03 | 24183491 | G | A | upstream_gene_variant | MODIFIER | c.-1740C>T| |
S36 |
15 | BAA03g50120 | A03 | 24183503 | C | T | upstream_gene_variant | MODIFIER | c.-1752G>A| |
S79 S91 |
16 | BAA03g50120 | A03 | 24184389 | G | A | upstream_gene_variant | MODIFIER | c.-2638C>T| |
S31 |
17 | BAA03g50120 | A03 | 24185088 | G | A | upstream_gene_variant | MODIFIER | c.-3337C>T| |
S1 S90 |
18 | BAA03g50120 | A03 | 24185698 | C | T | upstream_gene_variant | MODIFIER | c.-3947G>A| |
S251 |