Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20700 | A06 | 11033480 | T | C | missense_variant | MODERATE | c.44A>G|p.Glu15Gly |
S131 |
2 | BAA06g20700 | A06 | 11033751 | C | T | upstream_gene_variant | MODIFIER | c.-228G>A| |
S278 |
3 | BAA06g20700 | A06 | 11033856 | G | A | upstream_gene_variant | MODIFIER | c.-333C>T| |
S25 |
4 | BAA06g20700 | A06 | 11034535 | C | T | upstream_gene_variant | MODIFIER | c.-1012G>A| |
S252 |
5 | BAA06g20700 | A06 | 11034865 | G | A | upstream_gene_variant | MODIFIER | c.-1342C>T| |
S69 |
6 | BAA06g20700 | A06 | 11034869 | G | A | upstream_gene_variant | MODIFIER | c.-1346C>T| |
S283 |
7 | BAA06g20700 | A06 | 11035562 | C | T | upstream_gene_variant | MODIFIER | c.-2039G>A| |
S77 |
8 | BAA06g20700 | A06 | 11035935 | C | T | upstream_gene_variant | MODIFIER | c.-2412G>A| |
S144 |
9 | BAA06g20700 | A06 | 11036687 | C | T | upstream_gene_variant | MODIFIER | c.-3164G>A| |
S135 |
10 | BAA06g20700 | A06 | 11037819 | G | A | upstream_gene_variant | MODIFIER | c.-4296C>T| |
S246 |
11 | BAA06g20700 | A06 | 11038050 | G | A | upstream_gene_variant | MODIFIER | c.-4527C>T| |
S146 |
12 | BAA06g20700 | A06 | 11038427 | C | T | upstream_gene_variant | MODIFIER | c.-4904G>A| |
S278 |