Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20860 | A08 | 15953624 | C | T | missense_variant | MODERATE | c.923C>T|p.Ser308Phe |
S277 |
2 | BAA08g20860 | A08 | 15953996 | G | A | missense_variant | MODERATE | c.1220G>A|p.Arg407Lys |
S76 |
3 | BAA08g20860 | A08 | 15954495 | C | T | missense_variant | MODERATE | c.1570C>T|p.Leu524Phe |
S136 |
4 | BAA08g20860 | A08 | 15955275 | C | T | intron_variant | MODIFIER | c.2187+10C>T| |
S212 |
5 | BAA08g20860 | A08 | 15955420 | C | T | synonymous_variant | LOW | c.2262C>T|p.Asp754Asp |
S82 S92 |
6 | BAA08g20860 | A08 | 15955502 | G | A | missense_variant | MODERATE | c.2344G>A|p.Val782Ile |
S269 |
7 | BAA08g20860 | A08 | 15955649 | C | T | downstream_gene_variant | MODIFIER | c.*31C>T| |
S272 |
8 | BAA08g20860 | A08 | 15955832 | G | A | downstream_gene_variant | MODIFIER | c.*214G>A| |
S125 |
9 | BAA08g20860 | A08 | 15956265 | C | T | downstream_gene_variant | MODIFIER | c.*647C>T| |
S161 |
10 | BAA08g20860 | A08 | 15956692 | G | A | downstream_gene_variant | MODIFIER | c.*1074G>A| |
S100 |
11 | BAA08g20860 | A08 | 15956973 | G | A | downstream_gene_variant | MODIFIER | c.*1355G>A| |
S306 S308 |
12 | BAA08g20860 | A08 | 15958186 | C | T | downstream_gene_variant | MODIFIER | c.*2568C>T| |
S211 |
13 | BAA08g20860 | A08 | 15959713 | C | T | downstream_gene_variant | MODIFIER | c.*4095C>T| |
S139 |
14 | BAA08g20860 | A08 | 15959956 | G | A | downstream_gene_variant | MODIFIER | c.*4338G>A| |
S42 |
15 | BAA08g20860 | A08 | 15960218 | C | T | downstream_gene_variant | MODIFIER | c.*4600C>T| |
S206 S26 |