Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g15870 | A04 | 20494054 | C | T | upstream_gene_variant | MODIFIER | c.-3600C>T| |
S115 |
2 | BAA04g15870 | A04 | 20495222 | C | T | upstream_gene_variant | MODIFIER | c.-2432C>T| |
S299 |
3 | BAA04g15870 | A04 | 20495241 | G | A | upstream_gene_variant | MODIFIER | c.-2413G>A| |
S16 |
4 | BAA04g15870 | A04 | 20495384 | C | T | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S115 |
5 | BAA04g15870 | A04 | 20496782 | G | A | upstream_gene_variant | MODIFIER | c.-872G>A| |
S166 |
6 | BAA04g15870 | A04 | 20497129 | G | A | upstream_gene_variant | MODIFIER | c.-525G>A| |
S286 |
7 | BAA04g15870 | A04 | 20497320 | G | A | upstream_gene_variant | MODIFIER | c.-334G>A| |
S99 |
8 | BAA04g15870 | A04 | 20497980 | G | T | stop_gained | HIGH | c.235G>T|p.Glu79* |
S189 |
9 | BAA04g15870 | A04 | 20498758 | C | T | missense_variant | MODERATE | c.704C>T|p.Ala235Val |
S172 |
10 | BAA04g15870 | A04 | 20498790 | G | A | missense_variant | MODERATE | c.736G>A|p.Glu246Lys |
S183 S198 |
11 | BAA04g15870 | A04 | 20500120 | G | A | missense_variant | MODERATE | c.1441G>A|p.Val481Met |
S125 |
12 | BAA04g15870 | A04 | 20500316 | C | T | missense_variant | MODERATE | c.1538C>T|p.Thr513Ile |
S249 |
13 | BAA04g15870 | A04 | 20500324 | G | A | missense_variant | MODERATE | c.1546G>A|p.Asp516Asn |
S219 |
14 | BAA04g15870 | A04 | 20502102 | G | A | downstream_gene_variant | MODIFIER | c.*1761G>A| |
S11 |
15 | BAA04g15870 | A04 | 20502315 | T | A | downstream_gene_variant | MODIFIER | c.*1974T>A| |
S153 |
16 | BAA04g15870 | A04 | 20502750 | C | T | downstream_gene_variant | MODIFIER | c.*2409C>T| |
S216 |