Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06140 | A08 | 4853228 | G | A | downstream_gene_variant | MODIFIER | c.*4951C>T| |
S136 |
2 | BAA08g06140 | A08 | 4853281 | C | T | downstream_gene_variant | MODIFIER | c.*4898G>A| |
S133 |
3 | BAA08g06140 | A08 | 4854018 | G | A | downstream_gene_variant | MODIFIER | c.*4161C>T| |
S37 |
4 | BAA08g06140 | A08 | 4854961 | C | T | downstream_gene_variant | MODIFIER | c.*3218G>A| |
S112 |
5 | BAA08g06140 | A08 | 4856718 | C | T | downstream_gene_variant | MODIFIER | c.*1461G>A| |
S305 |
6 | BAA08g06140 | A08 | 4857868 | G | T | downstream_gene_variant | MODIFIER | c.*311C>A| |
S6 |
7 | BAA08g06140 | A08 | 4858282 | G | A | missense_variant | MODERATE | c.725C>T|p.Thr242Ile |
S122 |
8 | BAA08g06140 | A08 | 4859289 | G | A | intron_variant | MODIFIER | c.428-710C>T| |
S197 |
9 | BAA08g06140 | A08 | 4859345 | C | T | intron_variant | MODIFIER | c.428-766G>A| |
S66 |
10 | BAA08g06140 | A08 | 4861300 | C | T | missense_variant | MODERATE | c.388G>A|p.Gly130Arg |
S126 |
11 | BAA08g06140 | A08 | 4861338 | C | T | missense_variant | MODERATE | c.350G>A|p.Ser117Asn |
S162 |
12 | BAA08g06140 | A08 | 4861367 | G | A | synonymous_variant | LOW | c.321C>T|p.Ile107Ile |
S179 |
13 | BAA08g06140 | A08 | 4863963 | C | T | upstream_gene_variant | MODIFIER | c.-2014G>A| |
S157 S163 |
14 | BAA08g06140 | A08 | 4864564 | G | A | upstream_gene_variant | MODIFIER | c.-2615C>T| |
S297 |
15 | BAA08g06140 | A08 | 4864665 | G | A | upstream_gene_variant | MODIFIER | c.-2716C>T| |
S129 |
16 | BAA08g06140 | A08 | 4864745 | C | T | upstream_gene_variant | MODIFIER | c.-2796G>A| |
S152 |
17 | BAA08g06140 | A08 | 4864804 | C | T | upstream_gene_variant | MODIFIER | c.-2855G>A| |
S207 |
18 | BAA08g06140 | A08 | 4865689 | G | A | upstream_gene_variant | MODIFIER | c.-3740C>T| |
S139 |
19 | BAA08g06140 | A08 | 4865773 | G | A | upstream_gene_variant | MODIFIER | c.-3824C>T| |
S153 |