| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 140101 | BAA10g25250 | A10 | 20491479 | C | T | upstream_gene_variant | MODIFIER | c.-2669C>T| |
S265 S39 |
| 140102 | BAA10g25250 | A10 | 20491719 | C | T | upstream_gene_variant | MODIFIER | c.-2429C>T| |
S38 |
| 140103 | BAA10g25250 | A10 | 20492908 | G | A | upstream_gene_variant | MODIFIER | c.-1240G>A| |
S137 |
| 140104 | BAA10g25250 | A10 | 20493133 | C | T | upstream_gene_variant | MODIFIER | c.-1015C>T| |
S119 S44 |
| 140105 | BAA10g25250 | A10 | 20494131 | G | A | upstream_gene_variant | MODIFIER | c.-17G>A| |
S236 |
| 140106 | BAA10g25250 | A10 | 20494359 | C | T | missense_variant | MODERATE | c.212C>T|p.Ser71Phe |
S142 |
| 140107 | BAA10g25260 | A10 | 20495808 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S67 |
| 140108 | BAA10g25260 | A10 | 20496068 | G | A | missense_variant | MODERATE | c.160G>A|p.Glu54Lys |
S43 |
| 140109 | BAA10g25260 | A10 | 20496145 | C | T | synonymous_variant | LOW | c.237C>T|p.Ile79Ile |
S165 |
| 140110 | BAA10g25250 | A10 | 20496515 | G | A | downstream_gene_variant | MODIFIER | c.*2143G>A| |
S139 |
| 140111 | BAA10g25250 | A10 | 20496888 | C | T | downstream_gene_variant | MODIFIER | c.*2516C>T| |
S20 |
| 140112 | BAA10g25270 | A10 | 20497169 | C | T | synonymous_variant | LOW | c.1032G>A|p.Pro344Pro |
S154 S209 |
| 140113 | BAA10g25250 | A10 | 20497989 | C | T | downstream_gene_variant | MODIFIER | c.*3617C>T| |
S104 |
| 140114 | BAA10g25270 | A10 | 20498887 | G | A | upstream_gene_variant | MODIFIER | c.-91C>T| |
S223 |
| 140115 | BAA10g25270 | A10 | 20498947 | G | A | upstream_gene_variant | MODIFIER | c.-151C>T| |
S28 |
| 140116 | BAA10g25270 | A10 | 20499648 | G | A | upstream_gene_variant | MODIFIER | c.-852C>T| |
S65 |
| 140117 | BAA10g25270 | A10 | 20500061 | C | T | upstream_gene_variant | MODIFIER | c.-1265G>A| |
S47 |
| 140118 | BAA10g25270 | A10 | 20500108 | C | T | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S46 |
| 140119 | BAA10g25270 | A10 | 20500370 | G | A | upstream_gene_variant | MODIFIER | c.-1574C>T| |
S228 |
| 140120 | BAA10g25280 | A10 | 20500699 | G | A | missense_variant | MODERATE | c.803C>T|p.Thr268Ile |
S208 |
| 140121 | BAA10g25280 | A10 | 20501036 | C | T | missense_variant | MODERATE | c.466G>A|p.Gly156Ser |
S89 |
| 140122 | BAA10g25270 | A10 | 20501660 | G | A | upstream_gene_variant | MODIFIER | c.-2864C>T| |
S16 |
| 140123 | BAA10g25270 | A10 | 20501818 | C | T | upstream_gene_variant | MODIFIER | c.-3022G>A| |
S150 |
| 140124 | BAA10g25270 | A10 | 20502533 | G | A | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S159 S243 S276 S298 |
| 140125 | BAA10g25290 | A10 | 20503870 | C | T | splice_region_variant&intron_variant | LOW | c.654+6G>A| |
S301 S304 |