Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g26710 | A04 | 27172398 | G | A | upstream_gene_variant | MODIFIER | c.-4965G>A| |
S34 |
2 | BAA04g26710 | A04 | 27172566 | C | T | upstream_gene_variant | MODIFIER | c.-4797C>T| |
S203 |
3 | BAA04g26710 | A04 | 27173157 | C | T | upstream_gene_variant | MODIFIER | c.-4206C>T| |
S246 |
4 | BAA04g26710 | A04 | 27173777 | C | T | upstream_gene_variant | MODIFIER | c.-3586C>T| |
S8 |
5 | BAA04g26710 | A04 | 27174565 | C | T | upstream_gene_variant | MODIFIER | c.-2798C>T| |
S165 S211 S227 |
6 | BAA04g26710 | A04 | 27176958 | G | A | upstream_gene_variant | MODIFIER | c.-405G>A| |
S15 S3 |
7 | BAA04g26710 | A04 | 27177344 | C | T | upstream_gene_variant | MODIFIER | c.-19C>T| |
S132 S137 S215 |
8 | BAA04g26710 | A04 | 27177563 | C | T | synonymous_variant | LOW | c.201C>T|p.Ser67Ser |
S203 |
9 | BAA04g26710 | A04 | 27177996 | G | A | intron_variant | MODIFIER | c.483+10G>A| |
S108 |
10 | BAA04g26710 | A04 | 27178269 | C | T | synonymous_variant | LOW | c.624C>T|p.Leu208Leu |
S260 |
11 | BAA04g26710 | A04 | 27178571 | C | T | synonymous_variant | LOW | c.856C>T|p.Leu286Leu |
S125 |
12 | BAA04g26710 | A04 | 27178919 | G | A | missense_variant | MODERATE | c.1132G>A|p.Asp378Asn |
S259 |
13 | BAA04g26710 | A04 | 27179019 | T | G | missense_variant | MODERATE | c.1232T>G|p.Leu411Arg |
S151 S16 S40 |
14 | BAA04g26710 | A04 | 27179113 | G | A | intron_variant | MODIFIER | c.1262-19G>A| |
S179 |
15 | BAA04g26710 | A04 | 27179743 | G | A | missense_variant | MODERATE | c.1702G>A|p.Asp568Asn |
S99 |
16 | BAA04g26710 | A04 | 27179874 | G | T | missense_variant | MODERATE | c.1833G>T|p.Met611Ile |
S232 |
17 | BAA04g26710 | A04 | 27180217 | G | A | intron_variant | MODIFIER | c.1860-187G>A| |
S252 |
18 | BAA04g26710 | A04 | 27180342 | G | A | intron_variant | MODIFIER | c.1860-62G>A| |
S293 |
19 | BAA04g26710 | A04 | 27180776 | C | T | synonymous_variant | LOW | c.2232C>T|p.Ile744Ile |
S169 |
20 | BAA04g26710 | A04 | 27180826 | G | A | stop_gained | HIGH | c.2282G>A|p.Trp761* |
S175 |
21 | BAA04g26710 | A04 | 27180918 | G | A | missense_variant | MODERATE | c.2374G>A|p.Glu792Lys |
S273 |
22 | BAA04g26710 | A04 | 27181101 | G | A | missense_variant | MODERATE | c.2557G>A|p.Val853Ile |
S297 |
23 | BAA04g26710 | A04 | 27181544 | G | A | intron_variant | MODIFIER | c.2578-40G>A| |
S297 |
24 | BAA04g26710 | A04 | 27181829 | A | G | synonymous_variant | LOW | c.2823A>G|p.Leu941Leu |
S138 |
25 | BAA04g26710 | A04 | 27182104 | C | T | missense_variant | MODERATE | c.3098C>T|p.Pro1033Leu |
S4 |