Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g15870 | A05 | 8621671 | C | T | downstream_gene_variant | MODIFIER | c.*164G>A| |
S209 |
2 | BAA05g15870 | A05 | 8622572 | C | T | intron_variant | MODIFIER | c.2445-278G>A| |
S133 |
3 | BAA05g15870 | A05 | 8623675 | C | T | missense_variant | MODERATE | c.2128G>A|p.Asp710Asn |
S116 |
4 | BAA05g15870 | A05 | 8624049 | G | A | missense_variant | MODERATE | c.1754C>T|p.Ala585Val |
S225 S73 |
5 | BAA05g15870 | A05 | 8624159 | C | T | synonymous_variant | LOW | c.1644G>A|p.Gly548Gly |
S155 S211 |
6 | BAA05g15870 | A05 | 8624588 | G | A | intron_variant | MODIFIER | c.1432-130C>T| |
S148 S30 |
7 | BAA05g15870 | A05 | 8625264 | C | T | intron_variant | MODIFIER | c.1159-34G>A| |
S108 |
8 | BAA05g15870 | A05 | 8625278 | C | T | intron_variant | MODIFIER | c.1159-48G>A| |
S87 |
9 | BAA05g15870 | A05 | 8625407 | G | A | intron_variant | MODIFIER | c.1158+19C>T| |
S40 S49 |
10 | BAA05g15870 | A05 | 8625555 | C | T | synonymous_variant | LOW | c.1029G>A|p.Val343Val |
S273 |
11 | BAA05g15870 | A05 | 8625988 | G | A | missense_variant | MODERATE | c.929C>T|p.Ala310Val |
S297 |
12 | BAA05g15870 | A05 | 8626337 | G | A | intron_variant | MODIFIER | c.843+34C>T| |
S190 |
13 | BAA05g15870 | A05 | 8626619 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.682-1G>A| |
S281 |
14 | BAA05g15870 | A05 | 8628383 | C | T | intron_variant | MODIFIER | c.147+15G>A| |
S221 |
15 | BAA05g15870 | A05 | 8630199 | G | A | upstream_gene_variant | MODIFIER | c.-1655C>T| |
S124 |
16 | BAA05g15870 | A05 | 8630417 | C | T | upstream_gene_variant | MODIFIER | c.-1873G>A| |
S204 |
17 | BAA05g15870 | A05 | 8630969 | C | T | upstream_gene_variant | MODIFIER | c.-2425G>A| |
S198 |
18 | BAA05g15870 | A05 | 8631254 | C | T | upstream_gene_variant | MODIFIER | c.-2710G>A| |
S249 |
19 | BAA05g15870 | A05 | 8631443 | G | A | upstream_gene_variant | MODIFIER | c.-2899C>T| |
S298 |