Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59070 | A09 | 57400932 | G | A | splice_region_variant&intron_variant | LOW | c.1144-3C>T| |
S70 |
2 | BAA09g59070 | A09 | 57401623 | C | T | missense_variant | MODERATE | c.887G>A|p.Gly296Glu |
S155 S211 |
3 | BAA09g59070 | A09 | 57402503 | C | T | missense_variant | MODERATE | c.569G>A|p.Gly190Asp |
S87 |
4 | BAA09g59070 | A09 | 57403172 | G | A | splice_region_variant&intron_variant | LOW | c.323+7C>T| |
S38 |
5 | BAA09g59070 | A09 | 57403788 | G | A | synonymous_variant | LOW | c.33C>T|p.Ser11Ser |
S38 |
6 | BAA09g59070 | A09 | 57405115 | G | A | upstream_gene_variant | MODIFIER | c.-1295C>T| |
S263 |
7 | BAA09g59070 | A09 | 57405587 | C | T | upstream_gene_variant | MODIFIER | c.-1767G>A| |
S205 |
8 | BAA09g59070 | A09 | 57406470 | G | A | upstream_gene_variant | MODIFIER | c.-2650C>T| |
S165 |
9 | BAA09g59070 | A09 | 57406867 | G | A | upstream_gene_variant | MODIFIER | c.-3047C>T| |
S165 |
10 | BAA09g59070 | A09 | 57407924 | G | A | upstream_gene_variant | MODIFIER | c.-4104C>T| |
S266 |
11 | BAA09g59070 | A09 | 57408003 | C | T | upstream_gene_variant | MODIFIER | c.-4183G>A| |
S175 S177 |
12 | BAA09g59070 | A09 | 57408292 | C | T | upstream_gene_variant | MODIFIER | c.-4472G>A| |
S206 |
13 | BAA09g59070 | A09 | 57408565 | C | T | upstream_gene_variant | MODIFIER | c.-4745G>A| |
S139 |