Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g15120 | A07 | 22482848 | C | T | missense_variant | MODERATE | c.2716G>A|p.Glu906Lys |
S107 |
2 | BAA07g15120 | A07 | 22485124 | G | A | intron_variant | MODIFIER | c.2423+10C>T| |
S135 |
3 | BAA07g15120 | A07 | 22485198 | G | A | missense_variant | MODERATE | c.2359C>T|p.Arg787Cys |
S110 |
4 | BAA07g15120 | A07 | 22486012 | C | T | intron_variant | MODIFIER | c.2309-688G>A| |
S200 |
5 | BAA07g15120 | A07 | 22486592 | C | T | intron_variant | MODIFIER | c.2308+510G>A| |
S298 |
6 | BAA07g15120 | A07 | 22487466 | C | T | synonymous_variant | LOW | c.1944G>A|p.Glu648Glu |
S167 |
7 | BAA07g15120 | A07 | 22487474 | G | A | missense_variant | MODERATE | c.1936C>T|p.Leu646Phe |
S97 |
8 | BAA07g15120 | A07 | 22487594 | G | A | missense_variant | MODERATE | c.1816C>T|p.Pro606Ser |
S263 |
9 | BAA07g15120 | A07 | 22489366 | C | T | missense_variant | MODERATE | c.676G>A|p.Glu226Lys |
S293 |
10 | BAA07g15120 | A07 | 22489994 | G | A | synonymous_variant | LOW | c.48C>T|p.Gly16Gly |
S219 S72 |
11 | BAA07g15120 | A07 | 22490740 | G | A | upstream_gene_variant | MODIFIER | c.-699C>T| |
S31 |
12 | BAA07g15120 | A07 | 22490830 | G | A | upstream_gene_variant | MODIFIER | c.-789C>T| |
S117 |
13 | BAA07g15120 | A07 | 22491005 | C | T | upstream_gene_variant | MODIFIER | c.-964G>A| |
S262 |
14 | BAA07g15120 | A07 | 22491078 | G | A | upstream_gene_variant | MODIFIER | c.-1037C>T| |
S63 |
15 | BAA07g15120 | A07 | 22493920 | C | T | upstream_gene_variant | MODIFIER | c.-3879G>A| |
S233 |