Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14110 | A05 | 7392361 | C | T | downstream_gene_variant | MODIFIER | c.*4670G>A| |
S181 |
2 | BAA05g14110 | A05 | 7392673 | C | T | downstream_gene_variant | MODIFIER | c.*4358G>A| |
S305 |
3 | BAA05g14110 | A05 | 7394373 | A | T | downstream_gene_variant | MODIFIER | c.*2658T>A| |
S11 |
4 | BAA05g14110 | A05 | 7395688 | G | A | downstream_gene_variant | MODIFIER | c.*1343C>T| |
S282 |
5 | BAA05g14110 | A05 | 7396206 | C | T | downstream_gene_variant | MODIFIER | c.*825G>A| |
S271 |
6 | BAA05g14110 | A05 | 7396380 | C | T | downstream_gene_variant | MODIFIER | c.*651G>A| |
S189 |
7 | BAA05g14110 | A05 | 7396697 | C | T | downstream_gene_variant | MODIFIER | c.*334G>A| |
S155 S211 |
8 | BAA05g14110 | A05 | 7396908 | C | T | downstream_gene_variant | MODIFIER | c.*123G>A| |
S242 |
9 | BAA05g14110 | A05 | 7396985 | C | T | downstream_gene_variant | MODIFIER | c.*46G>A| |
S183 S198 |
10 | BAA05g14110 | A05 | 7397221 | C | T | missense_variant | MODERATE | c.1910G>A|p.Ser637Asn |
S180 |
11 | BAA05g14110 | A05 | 7397258 | G | A | missense_variant | MODERATE | c.1873C>T|p.Pro625Ser |
S212 |
12 | BAA05g14110 | A05 | 7397317 | C | T | missense_variant | MODERATE | c.1814G>A|p.Arg605Lys |
S289 S290 |
13 | BAA05g14110 | A05 | 7397602 | G | A | missense_variant | MODERATE | c.1652C>T|p.Thr551Ile |
S34 |
14 | BAA05g14110 | A05 | 7398377 | G | C | stop_gained | HIGH | c.1292C>G|p.Ser431* |
S244 S289 S290 |
15 | BAA05g14110 | A05 | 7399324 | C | T | intron_variant | MODIFIER | c.673+27G>A| |
S198 |
16 | BAA05g14110 | A05 | 7399497 | G | T | intron_variant | MODIFIER | c.585-58C>A| |
S286 |
17 | BAA05g14110 | A05 | 7399536 | G | A | intron_variant | MODIFIER | c.585-97C>T| |
S185 S273 |
18 | BAA05g14110 | A05 | 7399808 | G | A | synonymous_variant | LOW | c.507C>T|p.Ile169Ile |
S124 |
19 | BAA05g14110 | A05 | 7399819 | G | A | missense_variant | MODERATE | c.496C>T|p.Leu166Phe |
S125 |
20 | BAA05g14110 | A05 | 7400143 | G | A | missense_variant | MODERATE | c.172C>T|p.Leu58Phe |
S196 |
21 | BAA05g14110 | A05 | 7400884 | C | T | upstream_gene_variant | MODIFIER | c.-570G>A| |
S143 |
22 | BAA05g14110 | A05 | 7401137 | G | A | upstream_gene_variant | MODIFIER | c.-823C>T| |
S144 |
23 | BAA05g14110 | A05 | 7401217 | G | A | upstream_gene_variant | MODIFIER | c.-903C>T| |
S127 |
24 | BAA05g14110 | A05 | 7401266 | C | T | upstream_gene_variant | MODIFIER | c.-952G>A| |
S136 S287 |
25 | BAA05g14110 | A05 | 7401997 | C | T | upstream_gene_variant | MODIFIER | c.-1683G>A| |
S206 S26 |