Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g32490 | A05 | 34626014 | C | T | downstream_gene_variant | MODIFIER | c.*1593G>A| |
S13 |
2 | BAA05g32490 | A05 | 34626133 | G | A | downstream_gene_variant | MODIFIER | c.*1474C>T| |
S270 |
3 | BAA05g32490 | A05 | 34627625 | C | T | stop_gained | HIGH | c.2739G>A|p.Trp913* |
S276 |
4 | BAA05g32490 | A05 | 34628783 | C | T | synonymous_variant | LOW | c.2109G>A|p.Glu703Glu |
S195 |
5 | BAA05g32490 | A05 | 34631122 | G | A | synonymous_variant | LOW | c.1956C>T|p.Ile652Ile |
S210 S225 |
6 | BAA05g32490 | A05 | 34632231 | C | T | missense_variant | MODERATE | c.1303G>A|p.Gly435Arg |
S166 |
7 | BAA05g32490 | A05 | 34634107 | C | T | synonymous_variant | LOW | c.513G>A|p.Gly171Gly |
S17 |
8 | BAA05g32490 | A05 | 34634822 | C | T | intron_variant | MODIFIER | c.252-132G>A| |
S143 |
9 | BAA05g32490 | A05 | 34635399 | G | A | intron_variant | MODIFIER | c.252-709C>T| |
S231 |
10 | BAA05g32490 | A05 | 34637366 | G | A | intron_variant | MODIFIER | c.92-11C>T| |
S55 |
11 | BAA05g32490 | A05 | 34637765 | C | T | upstream_gene_variant | MODIFIER | c.-226G>A| |
S191 |
12 | BAA05g32490 | A05 | 34638562 | C | T | upstream_gene_variant | MODIFIER | c.-1023G>A| |
S111 |
13 | BAA05g32490 | A05 | 34640721 | G | A | upstream_gene_variant | MODIFIER | c.-3182C>T| |
S190 |
14 | BAA05g32490 | A05 | 34641803 | C | T | upstream_gene_variant | MODIFIER | c.-4264G>A| |
S274 |