Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22130 | A08 | 16707505 | G | A | downstream_gene_variant | MODIFIER | c.*4686C>T| |
S273 |
2 | BAA08g22130 | A08 | 16707673 | G | A | downstream_gene_variant | MODIFIER | c.*4518C>T| |
S87 |
3 | BAA08g22130 | A08 | 16709108 | C | T | downstream_gene_variant | MODIFIER | c.*3083G>A| |
S152 |
4 | BAA08g22130 | A08 | 16709515 | G | A | downstream_gene_variant | MODIFIER | c.*2676C>T| |
S297 |
5 | BAA08g22130 | A08 | 16709783 | A | T | downstream_gene_variant | MODIFIER | c.*2408T>A| |
S109 |
6 | BAA08g22130 | A08 | 16712517 | C | T | missense_variant | MODERATE | c.2029G>A|p.Val677Ile |
S156 |
7 | BAA08g22130 | A08 | 16712964 | C | T | missense_variant | MODERATE | c.1653G>A|p.Met551Ile |
S223 |
8 | BAA08g22130 | A08 | 16713155 | C | T | missense_variant | MODERATE | c.1462G>A|p.Glu488Lys |
S249 |
9 | BAA08g22130 | A08 | 16713292 | G | A | missense_variant | MODERATE | c.1325C>T|p.Ser442Leu |
S282 |
10 | BAA08g22130 | A08 | 16713508 | G | A | missense_variant | MODERATE | c.1109C>T|p.Ser370Phe |
S146 |
11 | BAA08g22130 | A08 | 16713837 | C | T | synonymous_variant | LOW | c.780G>A|p.Lys260Lys |
S74 |
12 | BAA08g22130 | A08 | 16714168 | G | A | missense_variant | MODERATE | c.449C>T|p.Ser150Leu |
S96 |
13 | BAA08g22130 | A08 | 16718872 | G | A | upstream_gene_variant | MODIFIER | c.-3798C>T| |
S150 |
14 | BAA08g22130 | A08 | 16718899 | G | A | upstream_gene_variant | MODIFIER | c.-3825C>T| |
S277 S66 |
15 | BAA08g22130 | A08 | 16719521 | C | T | upstream_gene_variant | MODIFIER | c.-4447G>A| |
S59 |
16 | BAA08g22130 | A08 | 16719541 | C | T | upstream_gene_variant | MODIFIER | c.-4467G>A| |
S251 S74 |
17 | BAA08g22130 | A08 | 16720011 | G | A | upstream_gene_variant | MODIFIER | c.-4937C>T| |
S38 |
18 | BAA08g22130 | A08 | 16720055 | G | A | upstream_gene_variant | MODIFIER | c.-4981C>T| |
S62 |