Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11030 | A09 | 6121117 | C | T | stop_gained | HIGH | c.1749G>A|p.Trp583* |
S76 |
2 | BAA09g11030 | A09 | 6121342 | C | T | synonymous_variant | LOW | c.1524G>A|p.Leu508Leu |
S188 S276 |
3 | BAA09g11030 | A09 | 6121346 | G | A | missense_variant | MODERATE | c.1520C>T|p.Ser507Leu |
S13 |
4 | BAA09g11030 | A09 | 6121504 | G | A | synonymous_variant | LOW | c.1362C>T|p.Leu454Leu |
S135 |
5 | BAA09g11030 | A09 | 6121536 | T | C | missense_variant | MODERATE | c.1330A>G|p.Lys444Glu |
S177 |
6 | BAA09g11030 | A09 | 6121689 | C | T | missense_variant | MODERATE | c.1177G>A|p.Val393Ile |
S176 |
7 | BAA09g11030 | A09 | 6121928 | C | T | missense_variant | MODERATE | c.938G>A|p.Gly313Glu |
S37 |
8 | BAA09g11030 | A09 | 6122076 | G | A | missense_variant | MODERATE | c.790C>T|p.Pro264Ser |
S167 |
9 | BAA09g11030 | A09 | 6122929 | G | A | missense_variant | MODERATE | c.152C>T|p.Thr51Met |
S219 S72 |
10 | BAA09g11030 | A09 | 6126316 | G | A | upstream_gene_variant | MODIFIER | c.-3236C>T| |
S32 |