Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g39870 | A09 | 47249473 | C | T | upstream_gene_variant | MODIFIER | c.-2506C>T| |
S183 S198 |
2 | BAA09g39870 | A09 | 47249500 | G | A | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S221 |
3 | BAA09g39870 | A09 | 47249586 | G | A | upstream_gene_variant | MODIFIER | c.-2393G>A| |
S298 |
4 | BAA09g39870 | A09 | 47252444 | G | A | missense_variant | MODERATE | c.466G>A|p.Ala156Thr |
S180 |
5 | BAA09g39870 | A09 | 47252699 | C | T | missense_variant | MODERATE | c.721C>T|p.Pro241Ser |
S149 |
6 | BAA09g39870 | A09 | 47252744 | C | T | missense_variant | MODERATE | c.766C>T|p.Pro256Ser |
S39 |
7 | BAA09g39870 | A09 | 47253169 | C | T | synonymous_variant | LOW | c.1191C>T|p.Asp397Asp |
S152 |
8 | BAA09g39870 | A09 | 47253176 | C | T | missense_variant | MODERATE | c.1198C>T|p.Pro400Ser |
S168 |
9 | BAA09g39870 | A09 | 47253924 | C | T | missense_variant | MODERATE | c.1946C>T|p.Ser649Leu |
S168 |
10 | BAA09g39870 | A09 | 47254001 | G | A | missense_variant | MODERATE | c.2023G>A|p.Ala675Thr |
S167 |
11 | BAA09g39870 | A09 | 47254347 | C | T | synonymous_variant | LOW | c.2175C>T|p.Arg725Arg |
S50 |
12 | BAA09g39870 | A09 | 47254618 | C | T | missense_variant | MODERATE | c.2446C>T|p.Arg816Trp |
S308 |
13 | BAA09g39870 | A09 | 47254646 | C | T | missense_variant | MODERATE | c.2474C>T|p.Ala825Val |
S202 |
14 | BAA09g39870 | A09 | 47255094 | G | A | synonymous_variant | LOW | c.2922G>A|p.Leu974Leu |
S175 S177 |
15 | BAA09g39870 | A09 | 47257765 | C | T | missense_variant | MODERATE | c.3592C>T|p.Pro1198Ser |
S64 |
16 | BAA09g39870 | A09 | 47258506 | C | T | downstream_gene_variant | MODIFIER | c.*685C>T| |
S278 |
17 | BAA09g39870 | A09 | 47258911 | C | T | downstream_gene_variant | MODIFIER | c.*1090C>T| |
S39 |