Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26690 | A01 | 14974433 | G | A | downstream_gene_variant | MODIFIER | c.*1923C>T| |
S266 |
2 | BAA01g26690 | A01 | 14974773 | C | T | downstream_gene_variant | MODIFIER | c.*1583G>A| |
S64 |
3 | BAA01g26690 | A01 | 14975329 | G | A | downstream_gene_variant | MODIFIER | c.*1027C>T| |
S175 |
4 | BAA01g26690 | A01 | 14976228 | C | T | downstream_gene_variant | MODIFIER | c.*128G>A| |
S249 |
5 | BAA01g26690 | A01 | 14976729 | C | T | missense_variant | MODERATE | c.1376G>A|p.Arg459Lys |
S146 |
6 | BAA01g26690 | A01 | 14976799 | C | T | missense_variant | MODERATE | c.1306G>A|p.Asp436Asn |
S192 |
7 | BAA01g26690 | A01 | 14977084 | G | A | missense_variant | MODERATE | c.1021C>T|p.Pro341Ser |
S92 |
8 | BAA01g26690 | A01 | 14977093 | G | A | missense_variant | MODERATE | c.1012C>T|p.Pro338Ser |
S138 |
9 | BAA01g26690 | A01 | 14977381 | C | T | missense_variant | MODERATE | c.724G>A|p.Asp242Asn |
S232 |
10 | BAA01g26690 | A01 | 14977518 | G | A | missense_variant | MODERATE | c.587C>T|p.Ser196Phe |
S63 |
11 | BAA01g26690 | A01 | 14977798 | C | T | missense_variant | MODERATE | c.307G>A|p.Glu103Lys |
S162 |
12 | BAA01g26690 | A01 | 14977814 | C | T | synonymous_variant | LOW | c.291G>A|p.Leu97Leu |
S128 S162 |
13 | BAA01g26690 | A01 | 14977822 | C | T | missense_variant | MODERATE | c.283G>A|p.Asp95Asn |
S211 S227 |
14 | BAA01g26690 | A01 | 14978073 | C | T | missense_variant | MODERATE | c.32G>A|p.Gly11Glu |
S67 |
15 | BAA01g26690 | A01 | 14978111 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S125 |
16 | BAA01g26690 | A01 | 14978155 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S33 |
17 | BAA01g26690 | A01 | 14979897 | G | A | upstream_gene_variant | MODIFIER | c.-1793C>T| |
S109 |
18 | BAA01g26690 | A01 | 14982821 | C | T | upstream_gene_variant | MODIFIER | c.-4717G>A| |
S255 |
19 | BAA01g26690 | A01 | 14983057 | G | A | upstream_gene_variant | MODIFIER | c.-4953C>T| |
S236 |