Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64920 | A09 | 60038835 | G | A | missense_variant | MODERATE | c.2125C>T|p.Leu709Phe |
S13 |
2 | BAA09g64920 | A09 | 60039554 | C | T | missense_variant | MODERATE | c.1672G>A|p.Ala558Thr |
S257 |
3 | BAA09g64920 | A09 | 60040634 | G | A | synonymous_variant | LOW | c.1071C>T|p.Leu357Leu |
S196 |
4 | BAA09g64920 | A09 | 60040727 | C | T | synonymous_variant | LOW | c.978G>A|p.Lys326Lys |
S117 |
5 | BAA09g64920 | A09 | 60040974 | G | A | missense_variant | MODERATE | c.731C>T|p.Ser244Phe |
S13 |
6 | BAA09g64920 | A09 | 60041127 | C | T | missense_variant | MODERATE | c.578G>A|p.Gly193Glu |
S292 |
7 | BAA09g64920 | A09 | 60041229 | C | T | missense_variant | MODERATE | c.476G>A|p.Gly159Glu |
S103 |
8 | BAA09g64920 | A09 | 60043296 | G | A | upstream_gene_variant | MODIFIER | c.-1500C>T| |
S288 |
9 | BAA09g64920 | A09 | 60043493 | C | T | upstream_gene_variant | MODIFIER | c.-1697G>A| |
S20 |
10 | BAA09g64920 | A09 | 60043582 | G | A | upstream_gene_variant | MODIFIER | c.-1786C>T| |
S210 S225 |
11 | BAA09g64920 | A09 | 60044206 | G | A | upstream_gene_variant | MODIFIER | c.-2410C>T| |
S261 |
12 | BAA09g64920 | A09 | 60044461 | G | A | upstream_gene_variant | MODIFIER | c.-2665C>T| |
S2 |
13 | BAA09g64920 | A09 | 60044720 | C | T | upstream_gene_variant | MODIFIER | c.-2924G>A| |
S174 |
14 | BAA09g64920 | A09 | 60045203 | G | A | upstream_gene_variant | MODIFIER | c.-3407C>T| |
S128 |
15 | BAA09g64920 | A09 | 60045488 | C | T | upstream_gene_variant | MODIFIER | c.-3692G>A| |
S270 |