Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64700 | A09 | 59934592 | C | T | downstream_gene_variant | MODIFIER | c.*3233G>A| |
S103 |
2 | BAA09g64700 | A09 | 59934763 | G | A | downstream_gene_variant | MODIFIER | c.*3062C>T| |
S84 S93 |
3 | BAA09g64700 | A09 | 59934817 | C | T | downstream_gene_variant | MODIFIER | c.*3008G>A| |
S37 |
4 | BAA09g64700 | A09 | 59935336 | C | T | downstream_gene_variant | MODIFIER | c.*2489G>A| |
S87 |
5 | BAA09g64700 | A09 | 59935418 | C | T | downstream_gene_variant | MODIFIER | c.*2407G>A| |
S56 |
6 | BAA09g64700 | A09 | 59938199 | C | T | missense_variant | MODERATE | c.1192G>A|p.Val398Met |
S138 |
7 | BAA09g64700 | A09 | 59938341 | C | T | intron_variant | MODIFIER | c.1087-37G>A| |
S26 |
8 | BAA09g64700 | A09 | 59938509 | C | T | intron_variant | MODIFIER | c.1086+160G>A| |
S131 |
9 | BAA09g64700 | A09 | 59939089 | G | A | synonymous_variant | LOW | c.666C>T|p.Leu222Leu |
S13 |
10 | BAA09g64700 | A09 | 59939170 | G | A | synonymous_variant | LOW | c.585C>T|p.Ile195Ile |
S283 |
11 | BAA09g64700 | A09 | 59939495 | G | A | intron_variant | MODIFIER | c.457-197C>T| |
S134 |
12 | BAA09g64700 | A09 | 59939938 | C | T | missense_variant | MODERATE | c.437G>A|p.Gly146Asp |
S296 |
13 | BAA09g64700 | A09 | 59940018 | G | A | synonymous_variant | LOW | c.357C>T|p.Leu119Leu |
S46 |
14 | BAA09g64700 | A09 | 59941073 | C | T | upstream_gene_variant | MODIFIER | c.-444G>A| |
S18 |
15 | BAA09g64700 | A09 | 59941701 | C | T | upstream_gene_variant | MODIFIER | c.-1072G>A| |
S129 |
16 | BAA09g64700 | A09 | 59941843 | G | A | upstream_gene_variant | MODIFIER | c.-1214C>T| |
S265 |
17 | BAA09g64700 | A09 | 59943743 | C | T | upstream_gene_variant | MODIFIER | c.-3114G>A| |
S35 |
18 | BAA09g64700 | A09 | 59943873 | C | T | upstream_gene_variant | MODIFIER | c.-3244G>A| |
S92 |