Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g27260 | A09 | 17806980 | G | A | upstream_gene_variant | MODIFIER | c.-781G>A| |
S1 S90 |
2 | BAA09g27260 | A09 | 17810327 | C | T | missense_variant | MODERATE | c.2177C>T|p.Ser726Phe |
S30 S31 |
3 | BAA09g27260 | A09 | 17810380 | G | A | missense_variant | MODERATE | c.2230G>A|p.Glu744Lys |
S130 |
4 | BAA09g27260 | A09 | 17812763 | G | A | intron_variant | MODIFIER | c.2662+1411G>A| |
S291 |
5 | BAA09g27260 | A09 | 17816266 | G | A | splice_donor_variant&intron_variant | HIGH | c.2924+1G>A| |
S181 |
6 | BAA09g27260 | A09 | 17816936 | C | T | missense_variant | MODERATE | c.3188C>T|p.Pro1063Leu |
S28 |
7 | BAA09g27260 | A09 | 17818266 | G | A | missense_variant&splice_region_variant | MODERATE | c.3949G>A|p.Glu1317Lys |
S251 |
8 | BAA09g27260 | A09 | 17818859 | C | T | missense_variant | MODERATE | c.4249C>T|p.Pro1417Ser |
S36 |
9 | BAA09g27260 | A09 | 17819255 | C | T | synonymous_variant | LOW | c.4497C>T|p.Pro1499Pro |
S71 |
10 | BAA09g27260 | A09 | 17819378 | G | A | missense_variant | MODERATE | c.4537G>A|p.Glu1513Lys |
S130 |
11 | BAA09g27260 | A09 | 17820085 | C | T | downstream_gene_variant | MODIFIER | c.*675C>T| |
S56 |
12 | BAA09g27260 | A09 | 17821643 | G | A | downstream_gene_variant | MODIFIER | c.*2233G>A| |
S42 |
13 | BAA09g27260 | A09 | 17821980 | G | A | downstream_gene_variant | MODIFIER | c.*2570G>A| |
S162 |