Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02550 | A02 | 1152649 | C | T | downstream_gene_variant | MODIFIER | c.*1619G>A| |
S142 |
2 | BAA02g02550 | A02 | 1153130 | C | T | downstream_gene_variant | MODIFIER | c.*1138G>A| |
S200 |
3 | BAA02g02550 | A02 | 1153451 | C | T | downstream_gene_variant | MODIFIER | c.*817G>A| |
S61 |
4 | BAA02g02550 | A02 | 1154812 | G | A | missense_variant | MODERATE | c.5915C>T|p.Ser1972Phe |
S293 |
5 | BAA02g02550 | A02 | 1156228 | C | T | missense_variant | MODERATE | c.4499G>A|p.Gly1500Glu |
S159 |
6 | BAA02g02550 | A02 | 1157125 | C | T | missense_variant | MODERATE | c.3602G>A|p.Gly1201Glu |
S277 |
7 | BAA02g02550 | A02 | 1157506 | C | T | missense_variant | MODERATE | c.3221G>A|p.Ser1074Asn |
S94 |
8 | BAA02g02550 | A02 | 1158022 | C | T | missense_variant | MODERATE | c.2705G>A|p.Gly902Glu |
S240 |
9 | BAA02g02550 | A02 | 1158370 | C | T | missense_variant | MODERATE | c.2357G>A|p.Gly786Glu |
S234 |
10 | BAA02g02550 | A02 | 1158547 | G | A | missense_variant | MODERATE | c.2180C>T|p.Ser727Leu |
S165 |
11 | BAA02g02550 | A02 | 1159368 | G | A | synonymous_variant | LOW | c.1359C>T|p.Pro453Pro |
S107 |
12 | BAA02g02550 | A02 | 1159603 | C | T | missense_variant | MODERATE | c.1124G>A|p.Ser375Asn |
S88 |
13 | BAA02g02550 | A02 | 1159730 | C | T | missense_variant | MODERATE | c.997G>A|p.Gly333Ser |
S15 S3 |
14 | BAA02g02550 | A02 | 1160145 | C | T | synonymous_variant | LOW | c.582G>A|p.Leu194Leu |
S61 |
15 | BAA02g02550 | A02 | 1161995 | G | A | upstream_gene_variant | MODIFIER | c.-388C>T| |
S107 |