Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g34040 | A08 | 22047891 | C | T | synonymous_variant | LOW | c.2790G>A|p.Leu930Leu |
S10 |
2 | BAA08g34040 | A08 | 22048045 | G | A | synonymous_variant | LOW | c.2733C>T|p.Leu911Leu |
S305 |
3 | BAA08g34040 | A08 | 22049030 | C | T | missense_variant | MODERATE | c.2182G>A|p.Gly728Arg |
S73 S91 |
4 | BAA08g34040 | A08 | 22051728 | C | T | missense_variant | MODERATE | c.929G>A|p.Arg310Lys |
S88 |
5 | BAA08g34040 | A08 | 22052153 | G | A | splice_region_variant&intron_variant | LOW | c.825-4C>T| |
S36 |
6 | BAA08g34040 | A08 | 22052250 | C | T | missense_variant | MODERATE | c.805G>A|p.Glu269Lys |
S13 |
7 | BAA08g34040 | A08 | 22053576 | C | T | synonymous_variant | LOW | c.396G>A|p.Pro132Pro |
S130 |
8 | BAA08g34040 | A08 | 22053851 | G | A | missense_variant | MODERATE | c.121C>T|p.Pro41Ser |
S115 |
9 | BAA08g34040 | A08 | 22053947 | G | A | missense_variant | MODERATE | c.25C>T|p.Pro9Ser |
S266 |
10 | BAA08g34040 | A08 | 22054051 | G | A | upstream_gene_variant | MODIFIER | c.-80C>T| |
S185 |
11 | BAA08g34040 | A08 | 22054509 | G | A | upstream_gene_variant | MODIFIER | c.-538C>T| |
S292 |
12 | BAA08g34040 | A08 | 22058091 | C | T | upstream_gene_variant | MODIFIER | c.-4120G>A| |
S143 |
13 | BAA08g34040 | A08 | 22058883 | G | A | upstream_gene_variant | MODIFIER | c.-4912C>T| |
S256 |
14 | BAA08g34040 | A08 | 22058920 | C | T | upstream_gene_variant | MODIFIER | c.-4949G>A| |
S142 |