Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g15660 | A06 | 7742813 | C | T | upstream_gene_variant | MODIFIER | c.-306C>T| |
S150 |
2 | BAA06g15660 | A06 | 7742885 | C | T | upstream_gene_variant | MODIFIER | c.-234C>T| |
S56 |
3 | BAA06g15660 | A06 | 7743194 | G | A | missense_variant | MODERATE | c.76G>A|p.Ala26Thr |
S92 |
4 | BAA06g15660 | A06 | 7743478 | G | A | synonymous_variant | LOW | c.360G>A|p.Arg120Arg |
S39 |
5 | BAA06g15660 | A06 | 7743640 | G | A | synonymous_variant | LOW | c.444G>A|p.Glu148Glu |
S270 |
6 | BAA06g15660 | A06 | 7744282 | G | A | stop_gained | HIGH | c.566G>A|p.Trp189* |
S211 S227 |
7 | BAA06g15660 | A06 | 7744774 | C | T | splice_region_variant&intron_variant | LOW | c.730-3C>T| |
S109 |
8 | BAA06g15660 | A06 | 7745720 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.994-1G>A| |
S230 |
9 | BAA06g15660 | A06 | 7746858 | G | A | missense_variant | MODERATE | c.1736G>A|p.Arg579Lys |
S110 |
10 | BAA06g15660 | A06 | 7746877 | G | A | synonymous_variant | LOW | c.1755G>A|p.Arg585Arg |
S190 |
11 | BAA06g15660 | A06 | 7747142 | G | A | missense_variant | MODERATE | c.2020G>A|p.Glu674Lys |
S110 |
12 | BAA06g15660 | A06 | 7747172 | G | A | missense_variant | MODERATE | c.2050G>A|p.Val684Ile |
S161 |
13 | BAA06g15660 | A06 | 7748541 | G | A | downstream_gene_variant | MODIFIER | c.*1172G>A| |
S161 |
14 | BAA06g15660 | A06 | 7748723 | C | T | downstream_gene_variant | MODIFIER | c.*1354C>T| |
S23 |