| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 120701 | BAA10g11950 | A10 | 13510218 | C | T | upstream_gene_variant | MODIFIER | c.-1183G>A| |
S174 |
| 120702 | BAA10g11970 | A10 | 13515228 | C | T | upstream_gene_variant | MODIFIER | c.-2067C>T| |
S239 |
| 120703 | BAA10g11960 | A10 | 13515798 | G | A | missense_variant | MODERATE | c.484C>T|p.Leu162Phe |
S125 |
| 120704 | BAA10g11960 | A10 | 13516099 | C | T | synonymous_variant | LOW | c.183G>A|p.Glu61Glu |
S157 |
| 120705 | BAA10g11960 | A10 | 13516622 | G | A | upstream_gene_variant | MODIFIER | c.-341C>T| |
S125 |
| 120706 | BAA10g11960 | A10 | 13516728 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S110 |
| 120707 | BAA10g11970 | A10 | 13517676 | C | T | missense_variant | MODERATE | c.382C>T|p.Pro128Ser |
S40 S49 |
| 120708 | BAA10g11960 | A10 | 13518096 | G | A | upstream_gene_variant | MODIFIER | c.-1815C>T| |
S293 |
| 120709 | BAA10g11960 | A10 | 13519432 | C | T | upstream_gene_variant | MODIFIER | c.-3151G>A| |
S116 |
| 120710 | BAA10g11960 | A10 | 13519674 | G | A | upstream_gene_variant | MODIFIER | c.-3393C>T| |
S174 S216 S241 S265 S39 |
| 120711 | BAA10g11960 | A10 | 13520186 | G | A | upstream_gene_variant | MODIFIER | c.-3905C>T| |
S262 |
| 120712 | BAA10g11960 | A10 | 13520190 | G | A | upstream_gene_variant | MODIFIER | c.-3909C>T| |
S45 |
| 120713 | BAA10g11980 | A10 | 13520835 | G | A | synonymous_variant | LOW | c.315C>T|p.Ile105Ile |
S273 |
| 120714 | BAA10g11960 | A10 | 13520947 | C | T | upstream_gene_variant | MODIFIER | c.-4666G>A| |
S42 |
| 120715 | BAA10g11980 | A10 | 13521846 | C | T | upstream_gene_variant | MODIFIER | c.-271G>A| |
S282 |
| 120716 | BAA10g11980 | A10 | 13521981 | G | A | upstream_gene_variant | MODIFIER | c.-406C>T| |
S60 |
| 120717 | BAA10g11980 | A10 | 13522185 | C | T | upstream_gene_variant | MODIFIER | c.-610G>A| |
S96 |
| 120718 | BAA10g11990 | A10 | 13522418 | C | T | synonymous_variant | LOW | c.1299G>A|p.Arg433Arg |
S249 |
| 120719 | BAA10g11990 | A10 | 13522573 | G | A | missense_variant | MODERATE | c.1144C>T|p.Pro382Ser |
S139 |
| 120720 | BAA10g11990 | A10 | 13522750 | C | T | missense_variant | MODERATE | c.967G>A|p.Val323Ile |
S84 S93 |
| 120721 | BAA10g11990 | A10 | 13523251 | G | A | missense_variant | MODERATE | c.565C>T|p.Leu189Phe |
S67 |
| 120722 | BAA10g11990 | A10 | 13523441 | C | T | synonymous_variant | LOW | c.375G>A|p.Arg125Arg |
S272 |
| 120723 | BAA10g11990 | A10 | 13523629 | G | A | synonymous_variant | LOW | c.187C>T|p.Leu63Leu |
S176 |
| 120724 | BAA10g11980 | A10 | 13524521 | C | T | upstream_gene_variant | MODIFIER | c.-2946G>A| |
S2 |
| 120725 | BAA10g11980 | A10 | 13525393 | C | T | upstream_gene_variant | MODIFIER | c.-3818G>A| |
S256 |