Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69850 | A09 | 62172054 | G | A | synonymous_variant | LOW | c.4824C>T|p.Ser1608Ser |
S208 S93 |
2 | BAA09g69850 | A09 | 62172443 | C | T | synonymous_variant | LOW | c.4530G>A|p.Thr1510Thr |
S133 |
3 | BAA09g69850 | A09 | 62173663 | G | A | synonymous_variant | LOW | c.3483C>T|p.Phe1161Phe |
S277 |
4 | BAA09g69850 | A09 | 62174028 | C | T | synonymous_variant | LOW | c.3201G>A|p.Arg1067Arg |
S83 S88 |
5 | BAA09g69850 | A09 | 62176436 | G | A | missense_variant | MODERATE | c.1561C>T|p.Pro521Ser |
S84 S93 |
6 | BAA09g69850 | A09 | 62176766 | C | T | missense_variant | MODERATE | c.1400G>A|p.Arg467Gln |
S70 |
7 | BAA09g69850 | A09 | 62176771 | C | T | synonymous_variant | LOW | c.1395G>A|p.Val465Val |
S198 |
8 | BAA09g69850 | A09 | 62177294 | C | T | missense_variant | MODERATE | c.964G>A|p.Asp322Asn |
S183 S198 |
9 | BAA09g69850 | A09 | 62177411 | C | T | missense_variant | MODERATE | c.847G>A|p.Gly283Arg |
S78 |
10 | BAA09g69850 | A09 | 62177802 | G | A | synonymous_variant | LOW | c.456C>T|p.Leu152Leu |
S148 S210 S30 S31 |
11 | BAA09g69850 | A09 | 62178073 | G | A | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S13 |
12 | BAA09g69850 | A09 | 62178357 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S277 |
13 | BAA09g69850 | A09 | 62180781 | C | T | upstream_gene_variant | MODIFIER | c.-2524G>A| |
S236 |
14 | BAA09g69850 | A09 | 62182098 | C | T | upstream_gene_variant | MODIFIER | c.-3841G>A| |
S103 |