Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00320 | A01 | 154278 | G | A | downstream_gene_variant | MODIFIER | c.*3135C>T| |
S293 |
2 | BAA01g00320 | A01 | 154344 | C | T | downstream_gene_variant | MODIFIER | c.*3069G>A| |
S46 |
3 | BAA01g00320 | A01 | 158139 | C | T | stop_gained | HIGH | c.2283G>A|p.Trp761* |
S135 |
4 | BAA01g00320 | A01 | 158249 | C | T | missense_variant | MODERATE | c.2237G>A|p.Gly746Glu |
S1 S90 |
5 | BAA01g00320 | A01 | 158293 | G | A | synonymous_variant | LOW | c.2193C>T|p.Leu731Leu |
S168 |
6 | BAA01g00320 | A01 | 158411 | G | A | missense_variant | MODERATE | c.2075C>T|p.Ser692Phe |
S186 |
7 | BAA01g00320 | A01 | 160161 | C | T | missense_variant | MODERATE | c.1339G>A|p.Ala447Thr |
S74 |
8 | BAA01g00320 | A01 | 161030 | G | A | missense_variant | MODERATE | c.1277C>T|p.Ala426Val |
S200 |
9 | BAA01g00320 | A01 | 161163 | C | A | missense_variant | MODERATE | c.1144G>T|p.Gly382Cys |
S237 |
10 | BAA01g00320 | A01 | 161563 | G | A | intron_variant | MODIFIER | c.934+146C>T| |
S15 S3 |
11 | BAA01g00320 | A01 | 161629 | G | A | intron_variant | MODIFIER | c.934+80C>T| |
S240 |
12 | BAA01g00320 | A01 | 161754 | C | T | missense_variant | MODERATE | c.889G>A|p.Val297Ile |
S138 |
13 | BAA01g00320 | A01 | 161861 | G | A | missense_variant | MODERATE | c.782C>T|p.Pro261Leu |
S44 |
14 | BAA01g00320 | A01 | 161979 | C | T | intron_variant | MODIFIER | c.769-105G>A| |
S260 |
15 | BAA01g00320 | A01 | 162153 | C | T | intron_variant | MODIFIER | c.769-279G>A| |
S203 |
16 | BAA01g00320 | A01 | 162159 | C | T | intron_variant | MODIFIER | c.769-285G>A| |
S100 |
17 | BAA01g00320 | A01 | 162358 | G | A | intron_variant | MODIFIER | c.769-484C>T| |
S83 S88 |
18 | BAA01g00320 | A01 | 162410 | G | A | intron_variant | MODIFIER | c.769-536C>T| |
S244 |
19 | BAA01g00320 | A01 | 162495 | C | T | intron_variant | MODIFIER | c.769-621G>A| |
S64 |
20 | BAA01g00320 | A01 | 162560 | G | A | intron_variant | MODIFIER | c.769-686C>T| |
S75 |
21 | BAA01g00320 | A01 | 164616 | C | T | missense_variant | MODERATE | c.536G>A|p.Cys179Tyr |
S246 |
22 | BAA01g00320 | A01 | 164618 | C | T | synonymous_variant | LOW | c.534G>A|p.Ser178Ser |
S128 |
23 | BAA01g00320 | A01 | 164622 | G | A | missense_variant | MODERATE | c.530C>T|p.Pro177Leu |
S296 |
24 | BAA01g00320 | A01 | 164856 | G | A | missense_variant | MODERATE | c.296C>T|p.Pro99Leu |
S89 |