Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g52060 | A09 | 54041761 | C | T | upstream_gene_variant | MODIFIER | c.-4313C>T| |
S149 |
2 | BAA09g52060 | A09 | 54042230 | G | A | upstream_gene_variant | MODIFIER | c.-3844G>A| |
S244 |
3 | BAA09g52060 | A09 | 54043122 | C | T | upstream_gene_variant | MODIFIER | c.-2952C>T| |
S103 |
4 | BAA09g52060 | A09 | 54044017 | C | T | upstream_gene_variant | MODIFIER | c.-2057C>T| |
S50 |
5 | BAA09g52060 | A09 | 54044145 | C | T | upstream_gene_variant | MODIFIER | c.-1929C>T| |
S159 |
6 | BAA09g52060 | A09 | 54044344 | C | T | upstream_gene_variant | MODIFIER | c.-1730C>T| |
S138 |
7 | BAA09g52060 | A09 | 54046624 | G | A | intron_variant | MODIFIER | c.135+416G>A| |
S197 |
8 | BAA09g52060 | A09 | 54047037 | C | T | intron_variant | MODIFIER | c.135+829C>T| |
S140 |
9 | BAA09g52060 | A09 | 54047340 | G | A | intron_variant | MODIFIER | c.136-591G>A| |
S221 |
10 | BAA09g52060 | A09 | 54047709 | C | T | intron_variant | MODIFIER | c.136-222C>T| |
S68 |
11 | BAA09g52060 | A09 | 54053186 | C | T | missense_variant | MODERATE | c.1160C>T|p.Pro387Leu |
S207 |
12 | BAA09g52060 | A09 | 54053836 | C | T | missense_variant | MODERATE | c.1565C>T|p.Ser522Phe |
S211 S227 |
13 | BAA09g52060 | A09 | 54054365 | G | A | downstream_gene_variant | MODIFIER | c.*345G>A| |
S181 |
14 | BAA09g52060 | A09 | 54054639 | G | A | downstream_gene_variant | MODIFIER | c.*619G>A| |
S69 |