Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g32890 | A03 | 15291146 | G | A | missense_variant | MODERATE | c.2353C>T|p.Leu785Phe |
S107 |
2 | BAA03g32890 | A03 | 15291259 | G | A | missense_variant | MODERATE | c.2240C>T|p.Ser747Phe |
S244 |
3 | BAA03g32890 | A03 | 15291278 | C | T | missense_variant | MODERATE | c.2221G>A|p.Asp741Asn |
S90 |
4 | BAA03g32890 | A03 | 15291677 | C | T | missense_variant | MODERATE | c.2051G>A|p.Arg684Lys |
S295 |
5 | BAA03g32890 | A03 | 15291732 | C | T | missense_variant | MODERATE | c.1996G>A|p.Asp666Asn |
S140 |
6 | BAA03g32890 | A03 | 15291947 | C | T | missense_variant | MODERATE | c.1858G>A|p.Asp620Asn |
S279 |
7 | BAA03g32890 | A03 | 15292357 | C | T | missense_variant | MODERATE | c.1525G>A|p.Ala509Thr |
S125 |
8 | BAA03g32890 | A03 | 15292502 | G | A | missense_variant | MODERATE | c.1457C>T|p.Ser486Phe |
S148 S210 S30 |
9 | BAA03g32890 | A03 | 15292778 | C | T | synonymous_variant | LOW | c.1272G>A|p.Lys424Lys |
S208 S93 |
10 | BAA03g32890 | A03 | 15293028 | G | A | missense_variant | MODERATE | c.1022C>T|p.Pro341Leu |
S107 |
11 | BAA03g32890 | A03 | 15293138 | G | A | synonymous_variant | LOW | c.912C>T|p.Tyr304Tyr |
S86 |
12 | BAA03g32890 | A03 | 15293181 | C | T | missense_variant | MODERATE | c.869G>A|p.Gly290Asp |
S46 |
13 | BAA03g32890 | A03 | 15294648 | A | C | upstream_gene_variant | MODIFIER | c.-599T>G| |
S241 |
14 | BAA03g32890 | A03 | 15295405 | G | A | upstream_gene_variant | MODIFIER | c.-1356C>T| |
S296 |
15 | BAA03g32890 | A03 | 15297131 | G | A | upstream_gene_variant | MODIFIER | c.-3082C>T| |
S219 |
16 | BAA03g32890 | A03 | 15297991 | C | T | upstream_gene_variant | MODIFIER | c.-3942G>A| |
S1 S90 |
17 | BAA03g32890 | A03 | 15298336 | G | A | upstream_gene_variant | MODIFIER | c.-4287C>T| |
S197 |
18 | BAA03g32890 | A03 | 15298864 | C | T | upstream_gene_variant | MODIFIER | c.-4815G>A| |
S125 |