Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05370 | A07 | 4753823 | G | A | downstream_gene_variant | MODIFIER | c.*4697C>T| |
S244 |
2 | BAA07g05370 | A07 | 4754884 | G | A | downstream_gene_variant | MODIFIER | c.*3636C>T| |
S263 |
3 | BAA07g05370 | A07 | 4755150 | G | A | downstream_gene_variant | MODIFIER | c.*3370C>T| |
S265 S27 S39 |
4 | BAA07g05370 | A07 | 4755624 | G | A | downstream_gene_variant | MODIFIER | c.*2896C>T| |
S118 S119 |
5 | BAA07g05370 | A07 | 4755649 | C | T | downstream_gene_variant | MODIFIER | c.*2871G>A| |
S116 |
6 | BAA07g05370 | A07 | 4755806 | G | A | downstream_gene_variant | MODIFIER | c.*2714C>T| |
S174 S216 |
7 | BAA07g05370 | A07 | 4757051 | C | T | downstream_gene_variant | MODIFIER | c.*1469G>A| |
S128 |
8 | BAA07g05370 | A07 | 4757112 | C | T | downstream_gene_variant | MODIFIER | c.*1408G>A| |
S77 S82 |
9 | BAA07g05370 | A07 | 4757622 | G | A | downstream_gene_variant | MODIFIER | c.*898C>T| |
S211 S227 |
10 | BAA07g05370 | A07 | 4758045 | C | T | downstream_gene_variant | MODIFIER | c.*475G>A| |
S13 |
11 | BAA07g05370 | A07 | 4758726 | G | A | synonymous_variant | LOW | c.265C>T|p.Leu89Leu |
S278 |
12 | BAA07g05370 | A07 | 4758758 | C | A | missense_variant | MODERATE | c.233G>T|p.Arg78Leu |
S125 S61 |
13 | BAA07g05370 | A07 | 4760393 | C | T | upstream_gene_variant | MODIFIER | c.-1403G>A| |
S217 S248 |
14 | BAA07g05370 | A07 | 4760875 | C | T | upstream_gene_variant | MODIFIER | c.-1885G>A| |
S236 |
15 | BAA07g05370 | A07 | 4760927 | C | T | upstream_gene_variant | MODIFIER | c.-1937G>A| |
S242 |
16 | BAA07g05370 | A07 | 4763012 | C | T | upstream_gene_variant | MODIFIER | c.-4022G>A| |
S16 |
17 | BAA07g05370 | A07 | 4763269 | C | T | upstream_gene_variant | MODIFIER | c.-4279G>A| |
S195 |
18 | BAA07g05370 | A07 | 4763868 | G | A | upstream_gene_variant | MODIFIER | c.-4878C>T| |
S223 |
19 | BAA07g05370 | A07 | 4763953 | C | T | upstream_gene_variant | MODIFIER | c.-4963G>A| |
S73 |