Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20770 | A06 | 11083095 | G | A | missense_variant | MODERATE | c.1135C>T|p.Pro379Ser |
S38 |
2 | BAA06g20770 | A06 | 11083673 | C | T | missense_variant | MODERATE | c.799G>A|p.Glu267Lys |
S259 |
3 | BAA06g20770 | A06 | 11084068 | G | A | missense_variant | MODERATE | c.484C>T|p.Arg162Cys |
S184 |
4 | BAA06g20770 | A06 | 11084175 | G | A | missense_variant | MODERATE | c.377C>T|p.Pro126Leu |
S226 |
5 | BAA06g20770 | A06 | 11084220 | G | A | missense_variant | MODERATE | c.332C>T|p.Ser111Phe |
S201 |
6 | BAA06g20770 | A06 | 11084382 | T | A | missense_variant | MODERATE | c.170A>T|p.Glu57Val |
S132 S137 S215 S89 |
7 | BAA06g20770 | A06 | 11087208 | C | T | upstream_gene_variant | MODIFIER | c.-2130G>A| |
S279 |
8 | BAA06g20770 | A06 | 11087593 | C | T | upstream_gene_variant | MODIFIER | c.-2515G>A| |
S155 S211 |
9 | BAA06g20770 | A06 | 11089034 | G | A | upstream_gene_variant | MODIFIER | c.-3956C>T| |
S201 |
10 | BAA06g20770 | A06 | 11089527 | C | T | upstream_gene_variant | MODIFIER | c.-4449G>A| |
S80 |
11 | BAA06g20770 | A06 | 11089555 | G | A | upstream_gene_variant | MODIFIER | c.-4477C>T| |
S108 |