Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11630 | A09 | 6526370 | C | T | upstream_gene_variant | MODIFIER | c.-3690C>T| |
S303 |
2 | BAA09g11630 | A09 | 6526997 | G | A | upstream_gene_variant | MODIFIER | c.-3063G>A| |
S198 |
3 | BAA09g11630 | A09 | 6527888 | C | T | upstream_gene_variant | MODIFIER | c.-2172C>T| |
S13 |
4 | BAA09g11630 | A09 | 6527992 | C | T | upstream_gene_variant | MODIFIER | c.-2068C>T| |
S302 |
5 | BAA09g11630 | A09 | 6528535 | G | A | upstream_gene_variant | MODIFIER | c.-1525G>A| |
S45 |
6 | BAA09g11630 | A09 | 6529591 | C | T | upstream_gene_variant | MODIFIER | c.-469C>T| |
S19 |
7 | BAA09g11630 | A09 | 6529942 | G | A | upstream_gene_variant | MODIFIER | c.-118G>A| |
S286 |
8 | BAA09g11630 | A09 | 6530942 | G | A | stop_gained | HIGH | c.483G>A|p.Trp161* |
S284 |
9 | BAA09g11630 | A09 | 6531676 | G | A | missense_variant | MODERATE | c.898G>A|p.Val300Met |
S301 S304 |
10 | BAA09g11630 | A09 | 6532711 | G | A | downstream_gene_variant | MODIFIER | c.*659G>A| |
S252 |
11 | BAA09g11630 | A09 | 6533832 | C | T | downstream_gene_variant | MODIFIER | c.*1780C>T| |
S179 |