Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g03860 | A03 | 1652696 | C | T | upstream_gene_variant | MODIFIER | c.-3269C>T| |
S45 |
2 | BAA03g03860 | A03 | 1653668 | G | A | upstream_gene_variant | MODIFIER | c.-2297G>A| |
S25 S264 |
3 | BAA03g03860 | A03 | 1657414 | C | T | synonymous_variant | LOW | c.795C>T|p.Arg265Arg |
S223 |
4 | BAA03g03860 | A03 | 1657622 | C | T | synonymous_variant | LOW | c.913C>T|p.Leu305Leu |
S113 |
5 | BAA03g03860 | A03 | 1657649 | C | T | missense_variant | MODERATE | c.940C>T|p.Pro314Ser |
S58 |
6 | BAA03g03860 | A03 | 1658032 | C | T | missense_variant | MODERATE | c.1072C>T|p.Pro358Ser |
S159 S243 |
7 | BAA03g03860 | A03 | 1658638 | G | A | synonymous_variant | LOW | c.1380G>A|p.Glu460Glu |
S212 |
8 | BAA03g03860 | A03 | 1658818 | C | T | synonymous_variant | LOW | c.1485C>T|p.Asp495Asp |
S53 |
9 | BAA03g03860 | A03 | 1658955 | G | A | missense_variant&splice_region_variant | MODERATE | c.1501G>A|p.Val501Met |
S261 |
10 | BAA03g03860 | A03 | 1659880 | G | A | missense_variant | MODERATE | c.1957G>A|p.Gly653Ser |
S148 S31 |
11 | BAA03g03860 | A03 | 1659925 | G | A | missense_variant | MODERATE | c.2002G>A|p.Gly668Arg |
S174 |
12 | BAA03g03860 | A03 | 1661043 | C | T | missense_variant | MODERATE | c.2632C>T|p.His878Tyr |
S295 |
13 | BAA03g03860 | A03 | 1661049 | G | A | missense_variant | MODERATE | c.2638G>A|p.Val880Ile |
S57 |
14 | BAA03g03860 | A03 | 1661108 | G | A | synonymous_variant | LOW | c.2697G>A|p.Pro899Pro |
S197 |