Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26140 | A09 | 16913268 | G | A | synonymous_variant | LOW | c.1680C>T|p.Val560Val |
S115 |
2 | BAA09g26140 | A09 | 16913399 | C | T | splice_region_variant&intron_variant | LOW | c.1652+4G>A| |
S30 S31 |
3 | BAA09g26140 | A09 | 16913983 | G | A | synonymous_variant | LOW | c.1524C>T|p.Arg508Arg |
S301 |
4 | BAA09g26140 | A09 | 16914030 | G | A | missense_variant | MODERATE | c.1477C>T|p.Pro493Ser |
S121 |
5 | BAA09g26140 | A09 | 16914431 | G | A | stop_gained | HIGH | c.1240C>T|p.Gln414* |
S167 |
6 | BAA09g26140 | A09 | 16914489 | C | T | synonymous_variant | LOW | c.1182G>A|p.Gly394Gly |
S6 |
7 | BAA09g26140 | A09 | 16914658 | C | T | missense_variant | MODERATE | c.1100G>A|p.Gly367Asp |
S191 |
8 | BAA09g26140 | A09 | 16915725 | G | A | missense_variant | MODERATE | c.383C>T|p.Ala128Val |
S1 S90 |
9 | BAA09g26140 | A09 | 16916882 | G | A | upstream_gene_variant | MODIFIER | c.-272C>T| |
S25 |
10 | BAA09g26140 | A09 | 16917948 | G | A | upstream_gene_variant | MODIFIER | c.-1338C>T| |
S295 |
11 | BAA09g26140 | A09 | 16917969 | G | A | upstream_gene_variant | MODIFIER | c.-1359C>T| |
S295 |
12 | BAA09g26140 | A09 | 16918489 | C | T | upstream_gene_variant | MODIFIER | c.-1879G>A| |
S204 |
13 | BAA09g26140 | A09 | 16918987 | C | T | upstream_gene_variant | MODIFIER | c.-2377G>A| |
S206 S26 |
14 | BAA09g26140 | A09 | 16919670 | G | A | upstream_gene_variant | MODIFIER | c.-3060C>T| |
S170 S281 |
15 | BAA09g26140 | A09 | 16921536 | G | A | upstream_gene_variant | MODIFIER | c.-4926C>T| |
S216 |