Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38210 | A09 | 46183177 | G | A | missense_variant&splice_region_variant | MODERATE | c.3848C>T|p.Ser1283Leu |
S46 |
2 | BAA09g38210 | A09 | 46184224 | C | T | missense_variant | MODERATE | c.3494G>A|p.Arg1165His |
S206 S26 |
3 | BAA09g38210 | A09 | 46186390 | C | T | intron_variant | MODIFIER | c.2826+48G>A| |
S120 |
4 | BAA09g38210 | A09 | 46186963 | C | T | intron_variant | MODIFIER | c.2650-260G>A| |
S94 |
5 | BAA09g38210 | A09 | 46187875 | G | A | intron_variant | MODIFIER | c.2295+48C>T| |
S283 |
6 | BAA09g38210 | A09 | 46187880 | C | T | intron_variant | MODIFIER | c.2295+43G>A| |
S87 |
7 | BAA09g38210 | A09 | 46188645 | G | A | synonymous_variant | LOW | c.1695C>T|p.Ile565Ile |
S130 |
8 | BAA09g38210 | A09 | 46189951 | G | A | synonymous_variant | LOW | c.876C>T|p.Phe292Phe |
S266 |
9 | BAA09g38210 | A09 | 46193206 | C | T | upstream_gene_variant | MODIFIER | c.-75G>A| |
S1 S90 |
10 | BAA09g38210 | A09 | 46193737 | C | T | upstream_gene_variant | MODIFIER | c.-606G>A| |
S28 |
11 | BAA09g38210 | A09 | 46193990 | C | T | upstream_gene_variant | MODIFIER | c.-859G>A| |
S28 |
12 | BAA09g38210 | A09 | 46195329 | G | A | upstream_gene_variant | MODIFIER | c.-2198C>T| |
S89 |
13 | BAA09g38210 | A09 | 46195572 | G | A | upstream_gene_variant | MODIFIER | c.-2441C>T| |
S150 S293 |
14 | BAA09g38210 | A09 | 46197980 | G | A | upstream_gene_variant | MODIFIER | c.-4849C>T| |
S65 |
15 | BAA09g38210 | A09 | 46197981 | G | A | upstream_gene_variant | MODIFIER | c.-4850C>T| |
S185 |