Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15610 | A09 | 8956674 | G | A | synonymous_variant | LOW | c.72G>A|p.Val24Val |
S11 |
2 | BAA09g15610 | A09 | 8956885 | G | A | missense_variant | MODERATE | c.283G>A|p.Glu95Lys |
S122 |
3 | BAA09g15610 | A09 | 8956957 | G | A | missense_variant | MODERATE | c.355G>A|p.Asp119Asn |
S42 |
4 | BAA09g15610 | A09 | 8957004 | G | A | synonymous_variant | LOW | c.402G>A|p.Glu134Glu |
S38 |
5 | BAA09g15610 | A09 | 8957634 | G | A | synonymous_variant | LOW | c.591G>A|p.Glu197Glu |
S203 |
6 | BAA09g15610 | A09 | 8958170 | C | T | missense_variant | MODERATE | c.1127C>T|p.Thr376Ile |
S242 |
7 | BAA09g15610 | A09 | 8958199 | C | T | synonymous_variant | LOW | c.1156C>T|p.Leu386Leu |
S295 |
8 | BAA09g15610 | A09 | 8958715 | G | A | missense_variant | MODERATE | c.1576G>A|p.Asp526Asn |
S144 |
9 | BAA09g15610 | A09 | 8964185 | C | T | missense_variant | MODERATE | c.2239C>T|p.Pro747Ser |
S282 |
10 | BAA09g15610 | A09 | 8964347 | C | T | synonymous_variant | LOW | c.2401C>T|p.Leu801Leu |
S176 |
11 | BAA09g15610 | A09 | 8967737 | G | A | stop_gained&splice_region_variant | HIGH | c.3273G>A|p.Trp1091* |
S47 |
12 | BAA09g15610 | A09 | 8967936 | G | A | missense_variant | MODERATE | c.3472G>A|p.Val1158Ile |
S130 |