Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33010 | A09 | 41598939 | G | A | downstream_gene_variant | MODIFIER | c.*2098C>T| |
S107 |
2 | BAA09g33010 | A09 | 41599533 | C | T | downstream_gene_variant | MODIFIER | c.*1504G>A| |
S275 |
3 | BAA09g33010 | A09 | 41600857 | C | T | downstream_gene_variant | MODIFIER | c.*180G>A| |
S296 |
4 | BAA09g33010 | A09 | 41601100 | C | T | synonymous_variant | LOW | c.1062G>A|p.Lys354Lys |
S293 |
5 | BAA09g33010 | A09 | 41601337 | C | T | splice_region_variant&intron_variant | LOW | c.1002+6G>A| |
S113 |
6 | BAA09g33010 | A09 | 41601399 | G | A | missense_variant | MODERATE | c.946C>T|p.Pro316Ser |
S196 |
7 | BAA09g33010 | A09 | 41601447 | C | T | missense_variant | MODERATE | c.898G>A|p.Ala300Thr |
S9 |
8 | BAA09g33010 | A09 | 41601765 | G | A | missense_variant | MODERATE | c.668C>T|p.Ser223Phe |
S288 |
9 | BAA09g33010 | A09 | 41602439 | G | A | missense_variant | MODERATE | c.233C>T|p.Ala78Val |
S155 S211 |
10 | BAA09g33010 | A09 | 41602671 | C | T | missense_variant | MODERATE | c.62G>A|p.Arg21His |
S295 |
11 | BAA09g33010 | A09 | 41602775 | C | T | upstream_gene_variant | MODIFIER | c.-43G>A| |
S283 |
12 | BAA09g33010 | A09 | 41603089 | C | T | upstream_gene_variant | MODIFIER | c.-357G>A| |
S191 |
13 | BAA09g33010 | A09 | 41603120 | G | A | upstream_gene_variant | MODIFIER | c.-388C>T| |
S282 |
14 | BAA09g33010 | A09 | 41603791 | G | A | upstream_gene_variant | MODIFIER | c.-1059C>T| |
S13 |
15 | BAA09g33010 | A09 | 41604364 | C | T | upstream_gene_variant | MODIFIER | c.-1632G>A| |
S277 |