Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02690 | A02 | 1221730 | G | A | synonymous_variant | LOW | c.2161C>T|p.Leu721Leu |
S176 |
2 | BAA02g02690 | A02 | 1221847 | C | T | missense_variant | MODERATE | c.2044G>A|p.Ala682Thr |
S81 S85 |
3 | BAA02g02690 | A02 | 1221871 | G | A | splice_region_variant&intron_variant | LOW | c.2026-6C>T| |
S158 |
4 | BAA02g02690 | A02 | 1223284 | C | T | missense_variant | MODERATE | c.1282G>A|p.Asp428Asn |
S281 |
5 | BAA02g02690 | A02 | 1223319 | C | T | missense_variant | MODERATE | c.1247G>A|p.Gly416Glu |
S117 |
6 | BAA02g02690 | A02 | 1223391 | G | A | missense_variant | MODERATE | c.1175C>T|p.Ser392Leu |
S158 |
7 | BAA02g02690 | A02 | 1223801 | G | A | missense_variant | MODERATE | c.862C>T|p.Pro288Ser |
S67 |
8 | BAA02g02690 | A02 | 1223810 | C | T | missense_variant | MODERATE | c.853G>A|p.Asp285Asn |
S250 |
9 | BAA02g02690 | A02 | 1223822 | C | T | missense_variant | MODERATE | c.841G>A|p.Glu281Lys |
S15 S3 |
10 | BAA02g02690 | A02 | 1224393 | G | A | synonymous_variant | LOW | c.270C>T|p.Cys90Cys |
S271 |
11 | BAA02g02690 | A02 | 1225119 | C | T | upstream_gene_variant | MODIFIER | c.-457G>A| |
S16 |
12 | BAA02g02690 | A02 | 1225680 | C | T | upstream_gene_variant | MODIFIER | c.-1018G>A| |
S119 |
13 | BAA02g02690 | A02 | 1226097 | G | A | upstream_gene_variant | MODIFIER | c.-1435C>T| |
S236 |
14 | BAA02g02690 | A02 | 1227350 | C | T | upstream_gene_variant | MODIFIER | c.-2688G>A| |
S228 S250 |