Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37570 | A02 | 32157030 | G | A | upstream_gene_variant | MODIFIER | c.-3244G>A| |
S259 |
2 | BAA02g37570 | A02 | 32158123 | G | A | upstream_gene_variant | MODIFIER | c.-2151G>A| |
S196 |
3 | BAA02g37570 | A02 | 32158608 | C | T | upstream_gene_variant | MODIFIER | c.-1666C>T| |
S38 |
4 | BAA02g37570 | A02 | 32159333 | G | A | upstream_gene_variant | MODIFIER | c.-941G>A| |
S207 |
5 | BAA02g37570 | A02 | 32159922 | G | A | upstream_gene_variant | MODIFIER | c.-352G>A| |
S155 |
6 | BAA02g37570 | A02 | 32160011 | C | T | upstream_gene_variant | MODIFIER | c.-263C>T| |
S289 S290 |
7 | BAA02g37570 | A02 | 32160698 | G | A | missense_variant | MODERATE | c.233G>A|p.Gly78Glu |
S293 |
8 | BAA02g37570 | A02 | 32160830 | C | T | missense_variant | MODERATE | c.365C>T|p.Ser122Phe |
S15 S3 |
9 | BAA02g37570 | A02 | 32160863 | G | A | missense_variant | MODERATE | c.398G>A|p.Gly133Glu |
S17 S218 S267 S269 |
10 | BAA02g37570 | A02 | 32161183 | A | C | missense_variant | MODERATE | c.418A>C|p.Met140Leu |
S189 S223 S256 S266 S35 |
11 | BAA02g37570 | A02 | 32161507 | T | G | intron_variant | MODIFIER | c.581-107T>G| |
S155 |
12 | BAA02g37570 | A02 | 32161508 | T | G | intron_variant | MODIFIER | c.581-106T>G| |
S155 |
13 | BAA02g37570 | A02 | 32161509 | T | G | intron_variant | MODIFIER | c.581-105T>G| |
S155 |
14 | BAA02g37570 | A02 | 32161655 | G | A | missense_variant | MODERATE | c.622G>A|p.Ala208Thr |
S207 |
15 | BAA02g37570 | A02 | 32162804 | G | A | intron_variant | MODIFIER | c.1158+16G>A| |
S190 |
16 | BAA02g37570 | A02 | 32164015 | C | T | intron_variant | MODIFIER | c.1722+71C>T| |
S296 |
17 | BAA02g37570 | A02 | 32164289 | C | T | splice_region_variant&intron_variant | LOW | c.1863+7C>T| |
S251 |
18 | BAA02g37570 | A02 | 32164460 | G | A | intron_variant | MODIFIER | c.1956+9G>A| |
S103 |
19 | BAA02g37570 | A02 | 32165247 | G | A | missense_variant | MODERATE | c.2434G>A|p.Val812Ile |
S34 |
20 | BAA02g37570 | A02 | 32165894 | C | T | missense_variant | MODERATE | c.2900C>T|p.Ala967Val |
S73 S91 |
21 | BAA02g37570 | A02 | 32166837 | G | A | intron_variant | MODIFIER | c.3419-38G>A| |
S228 |
22 | BAA02g37570 | A02 | 32167133 | G | A | synonymous_variant | LOW | c.3579G>A|p.Lys1193Lys |
S58 |
23 | BAA02g37570 | A02 | 32168178 | G | A | downstream_gene_variant | MODIFIER | c.*970G>A| |
S150 |
24 | BAA02g37570 | A02 | 32168754 | G | A | downstream_gene_variant | MODIFIER | c.*1546G>A| |
S294 |
25 | BAA02g37570 | A02 | 32168782 | G | A | downstream_gene_variant | MODIFIER | c.*1574G>A| |
S146 |