Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14960 | A05 | 7976205 | G | A | upstream_gene_variant | MODIFIER | c.-4605G>A| |
S94 |
2 | BAA05g14960 | A05 | 7976231 | C | T | upstream_gene_variant | MODIFIER | c.-4579C>T| |
S18 |
3 | BAA05g14960 | A05 | 7976630 | G | A | upstream_gene_variant | MODIFIER | c.-4180G>A| |
S3 |
4 | BAA05g14960 | A05 | 7980926 | G | A | synonymous_variant | LOW | c.117G>A|p.Ala39Ala |
S279 |
5 | BAA05g14960 | A05 | 7981081 | G | A | stop_gained | HIGH | c.272G>A|p.Trp91* |
S170 |
6 | BAA05g14960 | A05 | 7981202 | C | T | intron_variant | MODIFIER | c.299+94C>T| |
S95 |
7 | BAA05g14960 | A05 | 7984490 | G | A | missense_variant | MODERATE | c.575G>A|p.Gly192Glu |
S192 |
8 | BAA05g14960 | A05 | 7984771 | G | A | synonymous_variant | LOW | c.771G>A|p.Leu257Leu |
S123 |
9 | BAA05g14960 | A05 | 7985224 | C | T | missense_variant | MODERATE | c.1046C>T|p.Ala349Val |
S18 |
10 | BAA05g14960 | A05 | 7985317 | C | T | missense_variant | MODERATE | c.1139C>T|p.Ser380Phe |
S261 |
11 | BAA05g14960 | A05 | 7987664 | G | A | downstream_gene_variant | MODIFIER | c.*2334G>A| |
S11 |
12 | BAA05g14960 | A05 | 7988399 | C | T | downstream_gene_variant | MODIFIER | c.*3069C>T| |
S251 S28 |
13 | BAA05g14960 | A05 | 7988444 | C | T | downstream_gene_variant | MODIFIER | c.*3114C>T| |
S269 |