Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g04630 | A04 | 2909915 | C | T | upstream_gene_variant | MODIFIER | c.-1023C>T| |
S246 |
2 | BAA04g04630 | A04 | 2911106 | G | A | missense_variant | MODERATE | c.169G>A|p.Glu57Lys |
S236 |
3 | BAA04g04630 | A04 | 2911118 | G | A | missense_variant | MODERATE | c.181G>A|p.Glu61Lys |
S188 |
4 | BAA04g04630 | A04 | 2911255 | C | T | synonymous_variant | LOW | c.318C>T|p.Tyr106Tyr |
S186 |
5 | BAA04g04630 | A04 | 2911274 | G | A | missense_variant | MODERATE | c.337G>A|p.Val113Ile |
S207 |
6 | BAA04g04630 | A04 | 2911858 | G | A | splice_donor_variant&intron_variant | HIGH | c.621+1G>A| |
S286 |
7 | BAA04g04630 | A04 | 2912097 | C | T | missense_variant | MODERATE | c.760C>T|p.Leu254Phe |
S9 |
8 | BAA04g04630 | A04 | 2914171 | G | A | synonymous_variant | LOW | c.1227G>A|p.Glu409Glu |
S34 |
9 | BAA04g04630 | A04 | 2914624 | G | A | synonymous_variant | LOW | c.1590G>A|p.Ser530Ser |
S255 |
10 | BAA04g04630 | A04 | 2915567 | C | T | missense_variant | MODERATE | c.2294C>T|p.Ser765Leu |
S202 |
11 | BAA04g04630 | A04 | 2916011 | G | A | splice_region_variant&intron_variant | LOW | c.2731+7G>A| |
S256 |
12 | BAA04g04630 | A04 | 2916213 | G | A | synonymous_variant | LOW | c.2850G>A|p.Ser950Ser |
S184 |
13 | BAA04g04630 | A04 | 2916613 | C | T | synonymous_variant | LOW | c.3003C>T|p.Gly1001Gly |
S20 |
14 | BAA04g04630 | A04 | 2917136 | G | A | missense_variant | MODERATE | c.3526G>A|p.Val1176Ile |
S57 |
15 | BAA04g04630 | A04 | 2917413 | C | T | missense_variant | MODERATE | c.3803C>T|p.Ala1268Val |
S135 |
16 | BAA04g04630 | A04 | 2918855 | G | A | downstream_gene_variant | MODIFIER | c.*1042G>A| |
S280 |