Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00720 | A08 | 533258 | C | T | synonymous_variant | LOW | c.1311G>A|p.Ser437Ser |
S136 |
2 | BAA08g00720 | A08 | 533591 | C | T | missense_variant | MODERATE | c.1075G>A|p.Asp359Asn |
S134 |
3 | BAA08g00720 | A08 | 533843 | G | A | missense_variant | MODERATE | c.1037C>T|p.Ser346Leu |
S61 |
4 | BAA08g00720 | A08 | 533866 | G | A | synonymous_variant | LOW | c.1014C>T|p.Ile338Ile |
S11 |
5 | BAA08g00720 | A08 | 534002 | G | A | missense_variant | MODERATE | c.878C>T|p.Ser293Phe |
S146 |
6 | BAA08g00720 | A08 | 534324 | C | T | missense_variant | MODERATE | c.749G>A|p.Arg250Lys |
S302 |
7 | BAA08g00720 | A08 | 534551 | G | A | missense_variant | MODERATE | c.659C>T|p.Ala220Val |
S259 |
8 | BAA08g00720 | A08 | 535533 | G | A | missense_variant | MODERATE | c.83C>T|p.Thr28Ile |
S79 S91 |
9 | BAA08g00720 | A08 | 535878 | G | A | upstream_gene_variant | MODIFIER | c.-263C>T| |
S19 |
10 | BAA08g00720 | A08 | 536718 | G | A | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S166 S95 |
11 | BAA08g00720 | A08 | 536854 | G | T | upstream_gene_variant | MODIFIER | c.-1239C>A| |
S262 |
12 | BAA08g00720 | A08 | 537641 | G | A | upstream_gene_variant | MODIFIER | c.-2026C>T| |
S32 |