Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g37380 | A03 | 17246072 | C | T | upstream_gene_variant | MODIFIER | c.-382C>T| |
S176 |
2 | BAA03g37380 | A03 | 17247009 | G | A | missense_variant | MODERATE | c.556G>A|p.Ala186Thr |
S155 |
3 | BAA03g37380 | A03 | 17247056 | T | A | synonymous_variant | LOW | c.603T>A|p.Pro201Pro |
S299 |
4 | BAA03g37380 | A03 | 17247974 | G | A | synonymous_variant | LOW | c.1521G>A|p.Lys507Lys |
S86 |
5 | BAA03g37380 | A03 | 17248634 | G | A | synonymous_variant | LOW | c.2181G>A|p.Leu727Leu |
S83 S88 |
6 | BAA03g37380 | A03 | 17248669 | G | A | missense_variant | MODERATE | c.2216G>A|p.Gly739Glu |
S162 |
7 | BAA03g37380 | A03 | 17249434 | G | A | missense_variant | MODERATE | c.2536G>A|p.Glu846Lys |
S78 |
8 | BAA03g37380 | A03 | 17250102 | C | T | synonymous_variant | LOW | c.3126C>T|p.Phe1042Phe |
S105 S106 |
9 | BAA03g37380 | A03 | 17250145 | G | A | missense_variant | MODERATE | c.3169G>A|p.Gly1057Arg |
S260 |
10 | BAA03g37380 | A03 | 17250419 | G | A | missense_variant | MODERATE | c.3371G>A|p.Arg1124Lys |
S103 |
11 | BAA03g37380 | A03 | 17250574 | G | A | missense_variant | MODERATE | c.3526G>A|p.Val1176Met |
S104 S52 |
12 | BAA03g37380 | A03 | 17250974 | G | A | missense_variant | MODERATE | c.3811G>A|p.Gly1271Arg |
S119 |
13 | BAA03g37380 | A03 | 17251145 | G | A | missense_variant | MODERATE | c.3982G>A|p.Asp1328Asn |
S149 |
14 | BAA03g37380 | A03 | 17254087 | G | A | downstream_gene_variant | MODIFIER | c.*2287G>A| |
S123 |
15 | BAA03g37380 | A03 | 17254734 | C | T | downstream_gene_variant | MODIFIER | c.*2934C>T| |
S19 |
16 | BAA03g37380 | A03 | 17255164 | G | A | downstream_gene_variant | MODIFIER | c.*3364G>A| |
S287 |