Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g09140 | A01 | 4004863 | G | A | upstream_gene_variant | MODIFIER | c.-1050G>A| |
S203 |
2 | BAA01g09140 | A01 | 4006432 | C | T | missense_variant | MODERATE | c.520C>T|p.Pro174Ser |
S244 |
3 | BAA01g09140 | A01 | 4006538 | C | T | intron_variant | MODIFIER | c.602+24C>T| |
S198 |
4 | BAA01g09140 | A01 | 4008158 | C | T | missense_variant | MODERATE | c.1058C>T|p.Pro353Leu |
S152 |
5 | BAA01g09140 | A01 | 4008354 | C | T | synonymous_variant | LOW | c.1254C>T|p.Asp418Asp |
S250 |
6 | BAA01g09140 | A01 | 4008630 | C | T | downstream_gene_variant | MODIFIER | c.*255C>T| |
S66 |
7 | BAA01g09140 | A01 | 4008731 | C | T | downstream_gene_variant | MODIFIER | c.*356C>T| |
S263 |
8 | BAA01g09140 | A01 | 4008761 | G | A | downstream_gene_variant | MODIFIER | c.*386G>A| |
S12 |
9 | BAA01g09140 | A01 | 4009644 | G | A | downstream_gene_variant | MODIFIER | c.*1269G>A| |
S181 |
10 | BAA01g09140 | A01 | 4009766 | G | A | downstream_gene_variant | MODIFIER | c.*1391G>A| |
S34 |
11 | BAA01g09140 | A01 | 4011069 | G | A | downstream_gene_variant | MODIFIER | c.*2694G>A| |
S275 |
12 | BAA01g09140 | A01 | 4011381 | G | A | downstream_gene_variant | MODIFIER | c.*3006G>A| |
S262 |
13 | BAA01g09140 | A01 | 4011475 | C | T | downstream_gene_variant | MODIFIER | c.*3100C>T| |
S98 |
14 | BAA01g09140 | A01 | 4011621 | C | T | downstream_gene_variant | MODIFIER | c.*3246C>T| |
S10 |
15 | BAA01g09140 | A01 | 4012552 | C | T | downstream_gene_variant | MODIFIER | c.*4177C>T| |
S58 |