Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g43660 | A07 | 37309928 | C | T | missense_variant | MODERATE | c.1393G>A|p.Val465Met |
S279 |
2 | BAA07g43660 | A07 | 37310333 | C | T | missense_variant | MODERATE | c.1072G>A|p.Val358Ile |
S251 |
3 | BAA07g43660 | A07 | 37310957 | C | T | missense_variant | MODERATE | c.601G>A|p.Gly201Arg |
S107 |
4 | BAA07g43660 | A07 | 37312266 | C | T | intron_variant | MODIFIER | c.323+305G>A| |
S42 |
5 | BAA07g43660 | A07 | 37312763 | G | A | intron_variant | MODIFIER | c.232-101C>T| |
S140 |
6 | BAA07g43660 | A07 | 37313548 | C | T | intron_variant | MODIFIER | c.231+61G>A| |
S246 |
7 | BAA07g43660 | A07 | 37313610 | G | A | missense_variant&splice_region_variant | MODERATE | c.230C>T|p.Pro77Leu |
S262 |
8 | BAA07g43660 | A07 | 37313824 | G | A | intron_variant | MODIFIER | c.88-72C>T| |
S189 |
9 | BAA07g43660 | A07 | 37313906 | G | A | intron_variant | MODIFIER | c.87+66C>T| |
S202 |
10 | BAA07g43660 | A07 | 37313919 | G | A | intron_variant | MODIFIER | c.87+53C>T| |
S17 |
11 | BAA07g43660 | A07 | 37314908 | G | A | upstream_gene_variant | MODIFIER | c.-850C>T| |
S115 |
12 | BAA07g43660 | A07 | 37315507 | G | A | upstream_gene_variant | MODIFIER | c.-1449C>T| |
S95 |
13 | BAA07g43660 | A07 | 37316719 | C | A | upstream_gene_variant | MODIFIER | c.-2661G>T| |
S78 |
14 | BAA07g43660 | A07 | 37316721 | C | T | upstream_gene_variant | MODIFIER | c.-2663G>A| |
S293 |