Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g28440 | A06 | 19497260 | C | T | upstream_gene_variant | MODIFIER | c.-4419C>T| |
S107 |
2 | BAA06g28440 | A06 | 19497528 | G | A | upstream_gene_variant | MODIFIER | c.-4151G>A| |
S219 S72 |
3 | BAA06g28440 | A06 | 19497738 | G | A | upstream_gene_variant | MODIFIER | c.-3941G>A| |
S76 |
4 | BAA06g28440 | A06 | 19502118 | C | T | missense_variant | MODERATE | c.440C>T|p.Ser147Phe |
S165 S220 |
5 | BAA06g28440 | A06 | 19502164 | C | T | synonymous_variant | LOW | c.486C>T|p.Phe162Phe |
S282 |
6 | BAA06g28440 | A06 | 19502270 | G | A | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S183 S198 |
7 | BAA06g28440 | A06 | 19503991 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1844-1G>A| |
S185 |
8 | BAA06g28440 | A06 | 19504057 | G | A | missense_variant | MODERATE | c.1909G>A|p.Gly637Ser |
S262 |
9 | BAA06g28440 | A06 | 19504868 | C | T | missense_variant | MODERATE | c.2293C>T|p.Pro765Ser |
S259 |
10 | BAA06g28440 | A06 | 19504884 | C | T | missense_variant | MODERATE | c.2309C>T|p.Pro770Leu |
S62 |
11 | BAA06g28440 | A06 | 19505266 | G | A | missense_variant | MODERATE | c.2464G>A|p.Glu822Lys |
S283 |
12 | BAA06g28440 | A06 | 19508041 | G | A | downstream_gene_variant | MODIFIER | c.*2473G>A| |
S236 S260 |
13 | BAA06g28440 | A06 | 19508208 | G | A | downstream_gene_variant | MODIFIER | c.*2640G>A| |
S294 |
14 | BAA06g28440 | A06 | 19509394 | C | T | downstream_gene_variant | MODIFIER | c.*3826C>T| |
S113 |