Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g38090 | A05 | 37201469 | G | A | missense_variant | MODERATE | c.3503C>T|p.Ala1168Val |
S221 |
2 | BAA05g38090 | A05 | 37201947 | C | T | missense_variant | MODERATE | c.3025G>A|p.Glu1009Lys |
S173 |
3 | BAA05g38090 | A05 | 37201989 | C | T | missense_variant | MODERATE | c.2983G>A|p.Glu995Lys |
S13 S203 |
4 | BAA05g38090 | A05 | 37202221 | C | T | synonymous_variant | LOW | c.2751G>A|p.Ala917Ala |
S296 |
5 | BAA05g38090 | A05 | 37202544 | C | T | missense_variant | MODERATE | c.2428G>A|p.Glu810Lys |
S69 |
6 | BAA05g38090 | A05 | 37202617 | C | T | stop_gained | HIGH | c.2355G>A|p.Trp785* |
S72 |
7 | BAA05g38090 | A05 | 37204650 | C | T | missense_variant | MODERATE | c.2266G>A|p.Asp756Asn |
S178 |
8 | BAA05g38090 | A05 | 37205689 | G | A | missense_variant | MODERATE | c.1283C>T|p.Ala428Val |
S16 |
9 | BAA05g38090 | A05 | 37206233 | C | T | missense_variant | MODERATE | c.739G>A|p.Asp247Asn |
S94 |
10 | BAA05g38090 | A05 | 37206309 | C | T | synonymous_variant | LOW | c.663G>A|p.Glu221Glu |
S133 |
11 | BAA05g38090 | A05 | 37206482 | C | T | missense_variant | MODERATE | c.490G>A|p.Asp164Asn |
S69 |
12 | BAA05g38090 | A05 | 37206530 | C | T | missense_variant | MODERATE | c.442G>A|p.Gly148Arg |
S58 |
13 | BAA05g38090 | A05 | 37206835 | G | A | missense_variant | MODERATE | c.137C>T|p.Pro46Leu |
S124 |
14 | BAA05g38090 | A05 | 37207096 | C | T | upstream_gene_variant | MODIFIER | c.-125G>A| |
S19 |
15 | BAA05g38090 | A05 | 37210084 | C | T | upstream_gene_variant | MODIFIER | c.-3113G>A| |
S168 |
16 | BAA05g38090 | A05 | 37210180 | C | T | upstream_gene_variant | MODIFIER | c.-3209G>A| |
S13 S278 S279 S64 |
17 | BAA05g38090 | A05 | 37210704 | C | T | upstream_gene_variant | MODIFIER | c.-3733G>A| |
S94 |