Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41360 | A09 | 48131067 | C | T | missense_variant | MODERATE | c.4654G>A|p.Ala1552Thr |
S153 |
2 | BAA09g41360 | A09 | 48132328 | G | A | missense_variant | MODERATE | c.3700C>T|p.Pro1234Ser |
S225 S73 |
3 | BAA09g41360 | A09 | 48133226 | C | T | missense_variant&splice_region_variant | MODERATE | c.3032G>A|p.Arg1011Lys |
S58 |
4 | BAA09g41360 | A09 | 48133568 | G | A | synonymous_variant | LOW | c.2841C>T|p.Tyr947Tyr |
S48 |
5 | BAA09g41360 | A09 | 48133593 | G | A | missense_variant | MODERATE | c.2816C>T|p.Pro939Leu |
S75 S81 |
6 | BAA09g41360 | A09 | 48133891 | G | A | missense_variant | MODERATE | c.2765C>T|p.Pro922Leu |
S262 |
7 | BAA09g41360 | A09 | 48134686 | G | A | synonymous_variant | LOW | c.2124C>T|p.Ala708Ala |
S105 S106 |
8 | BAA09g41360 | A09 | 48134815 | G | A | missense_variant | MODERATE | c.2101C>T|p.Arg701Cys |
S194 |
9 | BAA09g41360 | A09 | 48135976 | G | A | missense_variant | MODERATE | c.1546C>T|p.Pro516Ser |
S226 |
10 | BAA09g41360 | A09 | 48136696 | C | T | missense_variant | MODERATE | c.983G>A|p.Gly328Asp |
S117 |
11 | BAA09g41360 | A09 | 48136831 | C | T | missense_variant | MODERATE | c.848G>A|p.Ser283Asn |
S168 |
12 | BAA09g41360 | A09 | 48138584 | G | A | upstream_gene_variant | MODIFIER | c.-696C>T| |
S246 |
13 | BAA09g41360 | A09 | 48138708 | C | T | upstream_gene_variant | MODIFIER | c.-820G>A| |
S297 |
14 | BAA09g41360 | A09 | 48139671 | C | T | upstream_gene_variant | MODIFIER | c.-1783G>A| |
S183 S198 |