Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g14790 | A04 | 19767511 | G | A | upstream_gene_variant | MODIFIER | c.-4695G>A| |
S288 |
2 | BAA04g14790 | A04 | 19768497 | G | A | upstream_gene_variant | MODIFIER | c.-3709G>A| |
S62 |
3 | BAA04g14790 | A04 | 19768598 | C | T | upstream_gene_variant | MODIFIER | c.-3608C>T| |
S299 |
4 | BAA04g14790 | A04 | 19769379 | C | T | upstream_gene_variant | MODIFIER | c.-2827C>T| |
S113 |
5 | BAA04g14790 | A04 | 19769754 | G | A | upstream_gene_variant | MODIFIER | c.-2452G>A| |
S171 |
6 | BAA04g14790 | A04 | 19770759 | C | T | upstream_gene_variant | MODIFIER | c.-1447C>T| |
S46 |
7 | BAA04g14790 | A04 | 19771015 | C | T | upstream_gene_variant | MODIFIER | c.-1191C>T| |
S167 |
8 | BAA04g14790 | A04 | 19771613 | G | A | upstream_gene_variant | MODIFIER | c.-593G>A| |
S56 |
9 | BAA04g14790 | A04 | 19772793 | C | T | synonymous_variant | LOW | c.588C>T|p.Thr196Thr |
S221 |
10 | BAA04g14790 | A04 | 19773050 | G | A | missense_variant | MODERATE | c.845G>A|p.Gly282Glu |
S195 |
11 | BAA04g14790 | A04 | 19773198 | G | A | synonymous_variant | LOW | c.993G>A|p.Gly331Gly |
S267 |
12 | BAA04g14790 | A04 | 19773276 | C | T | synonymous_variant | LOW | c.1071C>T|p.Asn357Asn |
S135 |
13 | BAA04g14790 | A04 | 19776172 | C | T | downstream_gene_variant | MODIFIER | c.*2752C>T| |
S74 |