Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g58670 | A03 | 29335749 | C | T | upstream_gene_variant | MODIFIER | c.-2353C>T| |
S130 |
2 | BAA03g58670 | A03 | 29338156 | G | A | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S10 |
3 | BAA03g58670 | A03 | 29339180 | G | A | missense_variant | MODERATE | c.713G>A|p.Gly238Glu |
S294 |
4 | BAA03g58670 | A03 | 29339748 | C | T | synonymous_variant | LOW | c.1281C>T|p.Ala427Ala |
S263 |
5 | BAA03g58670 | A03 | 29341585 | G | A | missense_variant | MODERATE | c.2675G>A|p.Ser892Asn |
S135 |
6 | BAA03g58670 | A03 | 29341926 | C | T | missense_variant | MODERATE | c.3016C>T|p.Leu1006Phe |
S32 |
7 | BAA03g58670 | A03 | 29342118 | G | A | missense_variant | MODERATE | c.3119G>A|p.Ser1040Asn |
S218 |
8 | BAA03g58670 | A03 | 29343320 | C | T | stop_gained | HIGH | c.4192C>T|p.Gln1398* |
S92 |
9 | BAA03g58670 | A03 | 29343798 | C | T | missense_variant | MODERATE | c.4670C>T|p.Ser1557Phe |
S288 |
10 | BAA03g58670 | A03 | 29344113 | C | T | missense_variant | MODERATE | c.4985C>T|p.Thr1662Ile |
S179 |
11 | BAA03g58670 | A03 | 29344644 | C | T | missense_variant | MODERATE | c.5402C>T|p.Ser1801Phe |
S118 |
12 | BAA03g58670 | A03 | 29345324 | G | A | downstream_gene_variant | MODIFIER | c.*379G>A| |
S64 |