Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g22550 | A06 | 12462031 | G | A | upstream_gene_variant | MODIFIER | c.-4377G>A| |
S149 S176 |
2 | BAA06g22550 | A06 | 12462151 | C | T | upstream_gene_variant | MODIFIER | c.-4257C>T| |
S216 S265 S39 S46 |
3 | BAA06g22550 | A06 | 12464785 | G | A | upstream_gene_variant | MODIFIER | c.-1623G>A| |
S236 |
4 | BAA06g22550 | A06 | 12465252 | C | T | upstream_gene_variant | MODIFIER | c.-1156C>T| |
S87 |
5 | BAA06g22550 | A06 | 12465645 | G | A | upstream_gene_variant | MODIFIER | c.-763G>A| |
S240 |
6 | BAA06g22550 | A06 | 12465879 | G | A | upstream_gene_variant | MODIFIER | c.-529G>A| |
S153 |
7 | BAA06g22550 | A06 | 12466352 | G | A | upstream_gene_variant | MODIFIER | c.-56G>A| |
S19 |
8 | BAA06g22550 | A06 | 12466401 | G | A | upstream_gene_variant | MODIFIER | c.-7G>A| |
S173 |
9 | BAA06g22550 | A06 | 12467085 | G | A | missense_variant | MODERATE | c.418G>A|p.Ala140Thr |
S82 S92 |
10 | BAA06g22550 | A06 | 12468048 | C | T | missense_variant | MODERATE | c.986C>T|p.Ala329Val |
S111 |
11 | BAA06g22550 | A06 | 12468078 | G | A | missense_variant | MODERATE | c.1016G>A|p.Ser339Asn |
S233 |
12 | BAA06g22550 | A06 | 12468803 | G | A | missense_variant | MODERATE | c.1366G>A|p.Asp456Asn |
S184 |
13 | BAA06g22550 | A06 | 12472081 | G | A | downstream_gene_variant | MODIFIER | c.*2501G>A| |
S125 |
14 | BAA06g22550 | A06 | 12473066 | G | A | downstream_gene_variant | MODIFIER | c.*3486G>A| |
S86 |
15 | BAA06g22550 | A06 | 12473780 | G | A | downstream_gene_variant | MODIFIER | c.*4200G>A| |
S146 |
16 | BAA06g22550 | A06 | 12473926 | C | T | downstream_gene_variant | MODIFIER | c.*4346C>T| |
S135 |