Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20330 | A10 | 18330495 | C | T | upstream_gene_variant | MODIFIER | c.-2358C>T| |
S244 |
2 | BAA10g20330 | A10 | 18330572 | C | T | upstream_gene_variant | MODIFIER | c.-2281C>T| |
S221 |
3 | BAA10g20330 | A10 | 18331567 | G | A | upstream_gene_variant | MODIFIER | c.-1286G>A| |
S160 |
4 | BAA10g20330 | A10 | 18333226 | G | A | missense_variant | MODERATE | c.163G>A|p.Glu55Lys |
S42 |
5 | BAA10g20330 | A10 | 18333906 | C | T | intron_variant | MODIFIER | c.582+33C>T| |
S122 |
6 | BAA10g20330 | A10 | 18334345 | G | A | intron_variant | MODIFIER | c.656-28G>A| |
S9 |
7 | BAA10g20330 | A10 | 18335328 | C | T | intron_variant | MODIFIER | c.999+238C>T| |
S157 S163 |
8 | BAA10g20330 | A10 | 18335920 | G | A | synonymous_variant | LOW | c.1134G>A|p.Glu378Glu |
S33 |
9 | BAA10g20330 | A10 | 18336253 | G | A | intron_variant | MODIFIER | c.1226+241G>A| |
S298 |
10 | BAA10g20330 | A10 | 18336655 | G | A | stop_gained | HIGH | c.1326G>A|p.Trp442* |
S212 |
11 | BAA10g20330 | A10 | 18337707 | G | A | synonymous_variant | LOW | c.1995G>A|p.Pro665Pro |
S46 |
12 | BAA10g20330 | A10 | 18339261 | C | T | missense_variant | MODERATE | c.3062C>T|p.Ala1021Val |
S161 |
13 | BAA10g20330 | A10 | 18339385 | C | T | synonymous_variant | LOW | c.3096C>T|p.Leu1032Leu |
S77 |
14 | BAA10g20330 | A10 | 18339404 | G | A | missense_variant | MODERATE | c.3115G>A|p.Glu1039Lys |
S272 |
15 | BAA10g20330 | A10 | 18340012 | C | T | missense_variant | MODERATE | c.3482C>T|p.Ala1161Val |
S26 |
16 | BAA10g20330 | A10 | 18341951 | G | A | missense_variant | MODERATE | c.4864G>A|p.Ala1622Thr |
S18 |