Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26930 | A01 | 15214003 | G | A | upstream_gene_variant | MODIFIER | c.-4727G>A| |
S103 |
2 | BAA01g26930 | A01 | 15215027 | G | A | upstream_gene_variant | MODIFIER | c.-3703G>A| |
S163 |
3 | BAA01g26930 | A01 | 15215147 | C | T | upstream_gene_variant | MODIFIER | c.-3583C>T| |
S155 S211 |
4 | BAA01g26930 | A01 | 15215530 | G | A | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S229 |
5 | BAA01g26930 | A01 | 15216479 | C | T | upstream_gene_variant | MODIFIER | c.-2251C>T| |
S177 |
6 | BAA01g26930 | A01 | 15216601 | G | A | upstream_gene_variant | MODIFIER | c.-2129G>A| |
S266 |
7 | BAA01g26930 | A01 | 15216873 | C | T | upstream_gene_variant | MODIFIER | c.-1857C>T| |
S183 |
8 | BAA01g26930 | A01 | 15217729 | G | A | upstream_gene_variant | MODIFIER | c.-1001G>A| |
S70 |
9 | BAA01g26930 | A01 | 15217825 | G | A | upstream_gene_variant | MODIFIER | c.-905G>A| |
S13 |
10 | BAA01g26930 | A01 | 15218047 | G | A | upstream_gene_variant | MODIFIER | c.-683G>A| |
S157 |
11 | BAA01g26930 | A01 | 15219063 | C | T | missense_variant | MODERATE | c.272C>T|p.Thr91Ile |
S10 |
12 | BAA01g26930 | A01 | 15219180 | C | T | splice_region_variant&intron_variant | LOW | c.322-5C>T| |
S44 |
13 | BAA01g26930 | A01 | 15219629 | G | A | missense_variant | MODERATE | c.685G>A|p.Gly229Arg |
S9 |
14 | BAA01g26930 | A01 | 15220341 | C | T | intron_variant | MODIFIER | c.1209+19C>T| |
S130 |
15 | BAA01g26930 | A01 | 15220505 | A | T | intron_variant | MODIFIER | c.1279+35A>T| |
S268 |
16 | BAA01g26930 | A01 | 15220821 | C | T | intron_variant | MODIFIER | c.1410+10C>T| |
S118 |
17 | BAA01g26930 | A01 | 15221259 | C | T | missense_variant | MODERATE | c.1610C>T|p.Ser537Leu |
S206 S26 |
18 | BAA01g26930 | A01 | 15221599 | G | A | missense_variant&splice_region_variant | MODERATE | c.1864G>A|p.Glu622Lys |
S278 |
19 | BAA01g26930 | A01 | 15221904 | G | A | intron_variant | MODIFIER | c.2029-27G>A| |
S157 |
20 | BAA01g26930 | A01 | 15221908 | C | T | intron_variant | MODIFIER | c.2029-23C>T| |
S66 |
21 | BAA01g26930 | A01 | 15222078 | G | A | intron_variant | MODIFIER | c.2137-33G>A| |
S56 |
22 | BAA01g26930 | A01 | 15222597 | C | T | missense_variant | MODERATE | c.2468C>T|p.Thr823Ile |
S20 |
23 | BAA01g26930 | A01 | 15223803 | C | T | downstream_gene_variant | MODIFIER | c.*112C>T| |
S203 |
24 | BAA01g26930 | A01 | 15224083 | G | A | downstream_gene_variant | MODIFIER | c.*392G>A| |
S86 |
25 | BAA01g26930 | A01 | 15224485 | C | T | downstream_gene_variant | MODIFIER | c.*794C>T| |
S272 |