Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17700 | A05 | 9990283 | G | A | synonymous_variant | LOW | c.2130C>T|p.Phe710Phe |
S157 S163 |
2 | BAA05g17700 | A05 | 9991598 | C | T | intron_variant | MODIFIER | c.1772-67G>A| |
S269 |
3 | BAA05g17700 | A05 | 9991640 | C | T | intron_variant | MODIFIER | c.1771+46G>A| |
S69 |
4 | BAA05g17700 | A05 | 9992065 | G | A | missense_variant | MODERATE | c.1492C>T|p.Leu498Phe |
S219 S72 |
5 | BAA05g17700 | A05 | 9993165 | G | A | intron_variant | MODIFIER | c.914+23C>T| |
S279 |
6 | BAA05g17700 | A05 | 9993403 | G | A | missense_variant | MODERATE | c.779C>T|p.Thr260Ile |
S76 |
7 | BAA05g17700 | A05 | 9993886 | C | T | intron_variant | MODIFIER | c.555-23G>A| |
S17 |
8 | BAA05g17700 | A05 | 9994274 | G | A | missense_variant | MODERATE | c.397C>T|p.Pro133Ser |
S216 |
9 | BAA05g17700 | A05 | 9995536 | G | A | intron_variant | MODIFIER | c.109+385C>T| |
S203 |
10 | BAA05g17700 | A05 | 9997271 | G | A | upstream_gene_variant | MODIFIER | c.-1242C>T| |
S86 |
11 | BAA05g17700 | A05 | 9997984 | C | T | upstream_gene_variant | MODIFIER | c.-1955G>A| |
S155 S211 |
12 | BAA05g17700 | A05 | 9998396 | G | A | upstream_gene_variant | MODIFIER | c.-2367C>T| |
S245 |
13 | BAA05g17700 | A05 | 10000685 | G | A | upstream_gene_variant | MODIFIER | c.-4656C>T| |
S150 |
14 | BAA05g17700 | A05 | 10000829 | G | A | upstream_gene_variant | MODIFIER | c.-4800C>T| |
S152 |