Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g28940 | A05 | 32652499 | C | T | downstream_gene_variant | MODIFIER | c.*2159G>A| |
S148 S210 S30 S31 |
2 | BAA05g28940 | A05 | 32654820 | C | T | synonymous_variant | LOW | c.3309G>A|p.Arg1103Arg |
S198 |
3 | BAA05g28940 | A05 | 32654842 | G | A | missense_variant | MODERATE | c.3287C>T|p.Thr1096Met |
S15 S3 |
4 | BAA05g28940 | A05 | 32655002 | C | T | missense_variant | MODERATE | c.3127G>A|p.Ala1043Thr |
S57 |
5 | BAA05g28940 | A05 | 32655175 | G | A | missense_variant | MODERATE | c.2954C>T|p.Ser985Phe |
S167 |
6 | BAA05g28940 | A05 | 32656322 | G | A | missense_variant | MODERATE | c.2191C>T|p.Pro731Ser |
S283 |
7 | BAA05g28940 | A05 | 32656408 | G | A | missense_variant | MODERATE | c.2105C>T|p.Thr702Ile |
S104 S52 |
8 | BAA05g28940 | A05 | 32656758 | G | A | synonymous_variant | LOW | c.1755C>T|p.His585His |
S138 |
9 | BAA05g28940 | A05 | 32657892 | G | A | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S240 |
10 | BAA05g28940 | A05 | 32657981 | C | T | missense_variant | MODERATE | c.800G>A|p.Arg267Lys |
S191 |
11 | BAA05g28940 | A05 | 32658742 | C | T | synonymous_variant | LOW | c.39G>A|p.Arg13Arg |
S156 S306 S308 |
12 | BAA05g28940 | A05 | 32658946 | G | A | upstream_gene_variant | MODIFIER | c.-82C>T| |
S264 |
13 | BAA05g28940 | A05 | 32659295 | G | A | upstream_gene_variant | MODIFIER | c.-431C>T| |
S308 |
14 | BAA05g28940 | A05 | 32661407 | A | C | upstream_gene_variant | MODIFIER | c.-2543T>G| |
S159 S168 S199 S205 S286 S70 S97 |
15 | BAA05g28940 | A05 | 32661567 | G | A | upstream_gene_variant | MODIFIER | c.-2703C>T| |
S1 |
16 | BAA05g28940 | A05 | 32661668 | G | A | upstream_gene_variant | MODIFIER | c.-2804C>T| |
S69 |
17 | BAA05g28940 | A05 | 32661929 | C | T | upstream_gene_variant | MODIFIER | c.-3065G>A| |
S286 |
18 | BAA05g28940 | A05 | 32663002 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S15 S3 |