Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g17170 | A04 | 21391395 | G | A | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S295 |
2 | BAA04g17170 | A04 | 21391454 | G | A | upstream_gene_variant | MODIFIER | c.-1776G>A| |
S79 S91 |
3 | BAA04g17170 | A04 | 21392265 | C | T | upstream_gene_variant | MODIFIER | c.-965C>T| |
S296 |
4 | BAA04g17170 | A04 | 21393209 | G | A | upstream_gene_variant | MODIFIER | c.-21G>A| |
S71 |
5 | BAA04g17170 | A04 | 21393366 | G | A | splice_region_variant&synonymous_variant | LOW | c.63G>A|p.Arg21Arg |
S40 S49 |
6 | BAA04g17170 | A04 | 21393585 | G | A | synonymous_variant | LOW | c.198G>A|p.Lys66Lys |
S133 |
7 | BAA04g17170 | A04 | 21393956 | C | T | missense_variant | MODERATE | c.569C>T|p.Thr190Ile |
S55 |
8 | BAA04g17170 | A04 | 21393972 | G | A | synonymous_variant | LOW | c.585G>A|p.Lys195Lys |
S59 |
9 | BAA04g17170 | A04 | 21394559 | C | T | missense_variant | MODERATE | c.1172C>T|p.Ala391Val |
S281 |
10 | BAA04g17170 | A04 | 21394866 | G | A | splice_region_variant&intron_variant | LOW | c.1192-7G>A| |
S15 S3 |
11 | BAA04g17170 | A04 | 21395144 | C | T | downstream_gene_variant | MODIFIER | c.*23C>T| |
S246 |
12 | BAA04g17170 | A04 | 21397165 | C | T | downstream_gene_variant | MODIFIER | c.*2044C>T| |
S205 |