Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26300 | A05 | 30989617 | C | T | upstream_gene_variant | MODIFIER | c.-4988C>T| |
S119 |
2 | BAA05g26300 | A05 | 30989807 | C | T | upstream_gene_variant | MODIFIER | c.-4798C>T| |
S94 |
3 | BAA05g26300 | A05 | 30989882 | C | T | upstream_gene_variant | MODIFIER | c.-4723C>T| |
S162 |
4 | BAA05g26300 | A05 | 30989896 | C | T | upstream_gene_variant | MODIFIER | c.-4709C>T| |
S68 |
5 | BAA05g26300 | A05 | 30991066 | C | T | upstream_gene_variant | MODIFIER | c.-3539C>T| |
S193 |
6 | BAA05g26300 | A05 | 30991670 | G | A | upstream_gene_variant | MODIFIER | c.-2935G>A| |
S10 |
7 | BAA05g26300 | A05 | 30992205 | A | T | upstream_gene_variant | MODIFIER | c.-2400A>T| |
S206 S208 S219 S230 S26 S63 S72 |
8 | BAA05g26300 | A05 | 30995766 | G | A | intron_variant | MODIFIER | c.313-169G>A| |
S296 |
9 | BAA05g26300 | A05 | 30995794 | G | A | intron_variant | MODIFIER | c.313-141G>A| |
S11 |
10 | BAA05g26300 | A05 | 30996309 | C | T | synonymous_variant | LOW | c.687C>T|p.Ser229Ser |
S99 |
11 | BAA05g26300 | A05 | 30997154 | A | G | intron_variant | MODIFIER | c.1314+14A>G| |
S28 |
12 | BAA05g26300 | A05 | 30997588 | C | T | missense_variant | MODERATE | c.1546C>T|p.Pro516Ser |
S13 S168 S219 S64 S72 |
13 | BAA05g26300 | A05 | 30997928 | G | A | intron_variant | MODIFIER | c.1696-12G>A| |
S90 |
14 | BAA05g26300 | A05 | 30998481 | C | T | downstream_gene_variant | MODIFIER | c.*161C>T| |
S269 |
15 | BAA05g26300 | A05 | 30998767 | G | A | downstream_gene_variant | MODIFIER | c.*447G>A| |
S13 |
16 | BAA05g26300 | A05 | 31001808 | C | T | downstream_gene_variant | MODIFIER | c.*3488C>T| |
S181 |
17 | BAA05g26300 | A05 | 31001981 | G | A | downstream_gene_variant | MODIFIER | c.*3661G>A| |
S265 |
18 | BAA05g26300 | A05 | 31002185 | G | A | downstream_gene_variant | MODIFIER | c.*3865G>A| |
S67 |
19 | BAA05g26300 | A05 | 31002789 | C | T | downstream_gene_variant | MODIFIER | c.*4469C>T| |
S69 |
20 | BAA05g26300 | A05 | 31003158 | G | A | downstream_gene_variant | MODIFIER | c.*4838G>A| |
S38 |