Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g28220 | A05 | 32197893 | G | A | upstream_gene_variant | MODIFIER | c.-3783G>A| |
S219 S72 |
2 | BAA05g28220 | A05 | 32198370 | G | A | upstream_gene_variant | MODIFIER | c.-3306G>A| |
S20 |
3 | BAA05g28220 | A05 | 32198567 | G | A | upstream_gene_variant | MODIFIER | c.-3109G>A| |
S211 S227 |
4 | BAA05g28220 | A05 | 32198847 | C | T | upstream_gene_variant | MODIFIER | c.-2829C>T| |
S292 |
5 | BAA05g28220 | A05 | 32199501 | C | T | upstream_gene_variant | MODIFIER | c.-2175C>T| |
S73 S91 |
6 | BAA05g28220 | A05 | 32201407 | G | A | upstream_gene_variant | MODIFIER | c.-269G>A| |
S166 |
7 | BAA05g28220 | A05 | 32202174 | C | T | missense_variant | MODERATE | c.499C>T|p.Pro167Ser |
S251 |
8 | BAA05g28220 | A05 | 32202271 | C | T | missense_variant | MODERATE | c.596C>T|p.Pro199Leu |
S182 |
9 | BAA05g28220 | A05 | 32202393 | C | T | missense_variant | MODERATE | c.718C>T|p.Pro240Ser |
S189 |
10 | BAA05g28220 | A05 | 32202668 | G | A | missense_variant | MODERATE | c.902G>A|p.Arg301His |
S11 |
11 | BAA05g28220 | A05 | 32203267 | G | A | missense_variant | MODERATE | c.1403G>A|p.Ser468Asn |
S104 S52 |
12 | BAA05g28220 | A05 | 32203277 | C | T | synonymous_variant | LOW | c.1413C>T|p.Val471Val |
S72 S78 |
13 | BAA05g28220 | A05 | 32204638 | G | A | downstream_gene_variant | MODIFIER | c.*1121G>A| |
S262 |
14 | BAA05g28220 | A05 | 32204885 | G | A | downstream_gene_variant | MODIFIER | c.*1368G>A| |
S76 |
15 | BAA05g28220 | A05 | 32204893 | G | A | downstream_gene_variant | MODIFIER | c.*1376G>A| |
S302 |
16 | BAA05g28220 | A05 | 32205571 | C | T | downstream_gene_variant | MODIFIER | c.*2054C>T| |
S153 |
17 | BAA05g28220 | A05 | 32206760 | C | T | downstream_gene_variant | MODIFIER | c.*3243C>T| |
S198 |
18 | BAA05g28220 | A05 | 32207271 | C | T | downstream_gene_variant | MODIFIER | c.*3754C>T| |
S171 |
19 | BAA05g28220 | A05 | 32208378 | C | T | downstream_gene_variant | MODIFIER | c.*4861C>T| |
S113 |