Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17530 | A09 | 10493041 | C | T | upstream_gene_variant | MODIFIER | c.-4353C>T| |
S18 |
2 | BAA09g17530 | A09 | 10493871 | G | A | upstream_gene_variant | MODIFIER | c.-3523G>A| |
S126 |
3 | BAA09g17530 | A09 | 10494348 | G | A | upstream_gene_variant | MODIFIER | c.-3046G>A| |
S121 |
4 | BAA09g17530 | A09 | 10494352 | G | A | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S155 S211 |
5 | BAA09g17530 | A09 | 10494434 | C | T | upstream_gene_variant | MODIFIER | c.-2960C>T| |
S122 |
6 | BAA09g17530 | A09 | 10494608 | C | T | upstream_gene_variant | MODIFIER | c.-2786C>T| |
S125 |
7 | BAA09g17530 | A09 | 10495008 | G | A | upstream_gene_variant | MODIFIER | c.-2386G>A| |
S171 |
8 | BAA09g17530 | A09 | 10495547 | G | A | upstream_gene_variant | MODIFIER | c.-1847G>A| |
S1 |
9 | BAA09g17530 | A09 | 10497772 | C | T | intron_variant | MODIFIER | c.37-96C>T| |
S132 S137 |
10 | BAA09g17530 | A09 | 10498110 | G | A | synonymous_variant | LOW | c.279G>A|p.Lys93Lys |
S57 |
11 | BAA09g17530 | A09 | 10499684 | C | T | missense_variant | MODERATE | c.1603C>T|p.Pro535Ser |
S39 |
12 | BAA09g17530 | A09 | 10501003 | G | A | missense_variant | MODERATE | c.2671G>A|p.Ala891Thr |
S271 |
13 | BAA09g17530 | A09 | 10501302 | C | T | downstream_gene_variant | MODIFIER | c.*264C>T| |
S186 S228 |
14 | BAA09g17530 | A09 | 10501698 | C | T | downstream_gene_variant | MODIFIER | c.*660C>T| |
S119 |