Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g31770 | A08 | 21041475 | C | T | downstream_gene_variant | MODIFIER | c.*2841G>A| |
S173 |
2 | BAA08g31770 | A08 | 21044912 | C | T | synonymous_variant | LOW | c.969G>A|p.Gly323Gly |
S70 |
3 | BAA08g31770 | A08 | 21044932 | G | A | missense_variant | MODERATE | c.949C>T|p.Pro317Ser |
S40 S49 |
4 | BAA08g31770 | A08 | 21045251 | G | T | synonymous_variant | LOW | c.630C>A|p.Leu210Leu |
S200 |
5 | BAA08g31770 | A08 | 21045512 | G | A | synonymous_variant | LOW | c.369C>T|p.Pro123Pro |
S78 |
6 | BAA08g31770 | A08 | 21045672 | C | A | missense_variant | MODERATE | c.209G>T|p.Gly70Val |
S107 S117 S170 S185 S297 |
7 | BAA08g31770 | A08 | 21047322 | C | T | upstream_gene_variant | MODIFIER | c.-1170G>A| |
S273 |
8 | BAA08g31770 | A08 | 21048688 | G | A | upstream_gene_variant | MODIFIER | c.-2536C>T| |
S246 |
9 | BAA08g31770 | A08 | 21049156 | C | T | upstream_gene_variant | MODIFIER | c.-3004G>A| |
S6 |
10 | BAA08g31770 | A08 | 21049643 | G | A | upstream_gene_variant | MODIFIER | c.-3491C>T| |
S155 S211 |
11 | BAA08g31770 | A08 | 21049796 | C | T | upstream_gene_variant | MODIFIER | c.-3644G>A| |
S57 |
12 | BAA08g31770 | A08 | 21050406 | G | A | upstream_gene_variant | MODIFIER | c.-4254C>T| |
S77 S82 |
13 | BAA08g31770 | A08 | 21050607 | G | A | upstream_gene_variant | MODIFIER | c.-4455C>T| |
S242 |
14 | BAA08g31770 | A08 | 21050696 | G | A | upstream_gene_variant | MODIFIER | c.-4544C>T| |
S139 |
15 | BAA08g31770 | A08 | 21050782 | G | A | upstream_gene_variant | MODIFIER | c.-4630C>T| |
S205 |
16 | BAA08g31770 | A08 | 21051007 | C | T | upstream_gene_variant | MODIFIER | c.-4855G>A| |
S210 S225 |