Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g07120 | A04 | 4740078 | G | A | missense_variant | MODERATE | c.121G>A|p.Val41Met |
S245 |
2 | BAA04g07120 | A04 | 4740139 | C | T | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S172 S217 |
3 | BAA04g07120 | A04 | 4740491 | C | T | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S45 |
4 | BAA04g07120 | A04 | 4740583 | C | T | missense_variant | MODERATE | c.571C>T|p.His191Tyr |
S268 |
5 | BAA04g07120 | A04 | 4740588 | G | A | synonymous_variant | LOW | c.576G>A|p.Pro192Pro |
S11 |
6 | BAA04g07120 | A04 | 4740793 | C | T | missense_variant | MODERATE | c.646C>T|p.Pro216Ser |
S272 |
7 | BAA04g07120 | A04 | 4741190 | C | T | missense_variant | MODERATE | c.1043C>T|p.Ser348Phe |
S156 |
8 | BAA04g07120 | A04 | 4741235 | G | A | missense_variant | MODERATE | c.1088G>A|p.Gly363Asp |
S131 |
9 | BAA04g07120 | A04 | 4742984 | C | T | intron_variant | MODIFIER | c.1122+1715C>T| |
S294 |
10 | BAA04g07120 | A04 | 4743319 | G | A | intron_variant | MODIFIER | c.1122+2050G>A| |
S5 |
11 | BAA04g07120 | A04 | 4743454 | G | A | intron_variant | MODIFIER | c.1123-1948G>A| |
S275 |
12 | BAA04g07120 | A04 | 4745408 | G | A | missense_variant | MODERATE | c.1129G>A|p.Glu377Lys |
S234 |
13 | BAA04g07120 | A04 | 4745479 | G | A | synonymous_variant | LOW | c.1200G>A|p.Leu400Leu |
S232 |
14 | BAA04g07120 | A04 | 4750141 | G | A | downstream_gene_variant | MODIFIER | c.*1678G>A| |
S126 |
15 | BAA04g07120 | A04 | 4751869 | C | T | downstream_gene_variant | MODIFIER | c.*3406C>T| |
S242 |