| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178751 | BAA02g19550 | A02 | 10156232 | G | A | downstream_gene_variant | MODIFIER | c.*288C>T| |
S263 |
| 178752 | BAA02g19550 | A02 | 10157110 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Ile |
S301 S304 |
| 178753 | BAA02g19550 | A02 | 10157233 | C | T | missense_variant | MODERATE | c.22G>A|p.Gly8Arg |
S209 |
| 178754 | BAA02g19550 | A02 | 10157503 | G | A | upstream_gene_variant | MODIFIER | c.-249C>T| |
S67 |
| 178755 | BAA02g19550 | A02 | 10157972 | C | T | upstream_gene_variant | MODIFIER | c.-718G>A| |
S216 |
| 178756 | BAA02g19550 | A02 | 10157976 | G | A | upstream_gene_variant | MODIFIER | c.-722C>T| |
S113 |
| 178757 | BAA02g19550 | A02 | 10158125 | G | A | upstream_gene_variant | MODIFIER | c.-871C>T| |
S67 |
| 178758 | BAA02g19550 | A02 | 10159819 | G | A | upstream_gene_variant | MODIFIER | c.-2565C>T| |
S265 |
| 178759 | BAA02g19550 | A02 | 10161323 | G | A | upstream_gene_variant | MODIFIER | c.-4069C>T| |
S217 S248 |
| 178760 | BAA02g19560 | A02 | 10162580 | C | T | upstream_gene_variant | MODIFIER | c.-430C>T| |
S144 |
| 178761 | BAA02g19560 | A02 | 10164360 | G | A | downstream_gene_variant | MODIFIER | c.*1183G>A| |
S48 |
| 178762 | BAA02g19560 | A02 | 10164995 | G | A | downstream_gene_variant | MODIFIER | c.*1818G>A| |
S293 |
| 178763 | BAA02g19560 | A02 | 10165032 | G | A | downstream_gene_variant | MODIFIER | c.*1855G>A| |
S122 |
| 178764 | BAA02g19570 | A02 | 10170170 | G | A | downstream_gene_variant | MODIFIER | c.*1934C>T| |
S92 |
| 178765 | BAA02g19570 | A02 | 10170945 | C | T | downstream_gene_variant | MODIFIER | c.*1159G>A| |
S156 S34 |
| 178766 | BAA02g19570 | A02 | 10171083 | G | A | downstream_gene_variant | MODIFIER | c.*1021C>T| |
S188 |
| 178767 | BAA02g19570 | A02 | 10172531 | C | T | intron_variant | MODIFIER | c.253-118G>A| |
S216 S241 S265 S39 |
| 178768 | BAA02g19570 | A02 | 10172834 | C | T | intron_variant | MODIFIER | c.143-27G>A| |
S71 |
| 178769 | BAA02g19570 | A02 | 10173177 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S35 |
| 178770 | BAA02g19570 | A02 | 10173243 | G | A | upstream_gene_variant | MODIFIER | c.-131C>T| |
S122 |
| 178771 | BAA02g19570 | A02 | 10173969 | G | A | upstream_gene_variant | MODIFIER | c.-857C>T| |
S33 |
| 178772 | BAA02g19570 | A02 | 10174369 | G | A | upstream_gene_variant | MODIFIER | c.-1257C>T| |
S11 |
| 178773 | BAA02g19570 | A02 | 10175079 | C | T | upstream_gene_variant | MODIFIER | c.-1967G>A| |
S171 |
| 178774 | BAA02g19570 | A02 | 10176163 | C | T | upstream_gene_variant | MODIFIER | c.-3051G>A| |
S205 |
| 178775 | BAA02g19570 | A02 | 10176265 | G | A | upstream_gene_variant | MODIFIER | c.-3153C>T| |
S202 |