Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g28050 | A08 | 19602984 | G | A | synonymous_variant | LOW | c.414G>A|p.Glu138Glu |
S202 |
2 | BAA08g28050 | A08 | 19603313 | G | A | missense_variant&splice_region_variant | MODERATE | c.566G>A|p.Gly189Asp |
S289 S290 |
3 | BAA08g28050 | A08 | 19604366 | C | T | missense_variant | MODERATE | c.1081C>T|p.Pro361Ser |
S172 |
4 | BAA08g28050 | A08 | 19604423 | G | A | splice_region_variant&intron_variant | LOW | c.1131+7G>A| |
S126 |
5 | BAA08g28050 | A08 | 19604871 | C | T | missense_variant | MODERATE | c.1313C>T|p.Ser438Phe |
S157 |
6 | BAA08g28050 | A08 | 19605697 | C | T | synonymous_variant | LOW | c.1788C>T|p.Ser596Ser |
S278 |
7 | BAA08g28050 | A08 | 19605719 | G | A | missense_variant | MODERATE | c.1810G>A|p.Val604Ile |
S150 |
8 | BAA08g28050 | A08 | 19607023 | C | T | downstream_gene_variant | MODIFIER | c.*1254C>T| |
S278 |
9 | BAA08g28050 | A08 | 19610293 | C | T | downstream_gene_variant | MODIFIER | c.*4524C>T| |
S249 |