| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 136901 | BAA10g22600-BAA10g22610 | A10 | 19355907 | C | T | intergenic_region | MODIFIER | n.19355907C>T| |
S68 |
| 136902 | BAA10g22610 | A10 | 19363102 | G | A | downstream_gene_variant | MODIFIER | c.*359G>A| |
S63 |
| 136903 | BAA10g22620 | A10 | 19364652 | G | A | upstream_gene_variant | MODIFIER | c.-4282G>A| |
S241 |
| 136904 | BAA10g22620 | A10 | 19365244 | G | A | upstream_gene_variant | MODIFIER | c.-3690G>A| |
S18 |
| 136905 | BAA10g22620 | A10 | 19366138 | C | T | upstream_gene_variant | MODIFIER | c.-2796C>T| |
S206 S26 |
| 136906 | BAA10g22620 | A10 | 19366235 | C | T | upstream_gene_variant | MODIFIER | c.-2699C>T| |
S183 |
| 136907 | BAA10g22620 | A10 | 19370155 | G | A | downstream_gene_variant | MODIFIER | c.*700G>A| |
S289 S290 |
| 136908 | BAA10g22620 | A10 | 19370157 | G | A | downstream_gene_variant | MODIFIER | c.*702G>A| |
S136 |
| 136909 | BAA10g22630 | A10 | 19372917 | T | A | upstream_gene_variant | MODIFIER | c.-3049T>A| |
S196 |
| 136910 | BAA10g22630 | A10 | 19372940 | C | T | upstream_gene_variant | MODIFIER | c.-3026C>T| |
S10 |
| 136911 | BAA10g22630 | A10 | 19373326 | C | T | upstream_gene_variant | MODIFIER | c.-2640C>T| |
S169 |
| 136912 | BAA10g22630 | A10 | 19373406 | G | A | upstream_gene_variant | MODIFIER | c.-2560G>A| |
S112 |
| 136913 | BAA10g22630 | A10 | 19373519 | G | A | upstream_gene_variant | MODIFIER | c.-2447G>A| |
S59 |
| 136914 | BAA10g22630 | A10 | 19374240 | G | A | upstream_gene_variant | MODIFIER | c.-1726G>A| |
S265 |
| 136915 | BAA10g22630 | A10 | 19375348 | C | T | upstream_gene_variant | MODIFIER | c.-618C>T| |
S183 |
| 136916 | BAA10g22630 | A10 | 19375730 | C | T | upstream_gene_variant | MODIFIER | c.-236C>T| |
S23 |
| 136917 | BAA10g22630 | A10 | 19375944 | C | T | upstream_gene_variant | MODIFIER | c.-22C>T| |
S77 S82 |
| 136918 | BAA10g22630 | A10 | 19376860 | C | T | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S275 |
| 136919 | BAA10g22630 | A10 | 19376955 | G | A | missense_variant | MODERATE | c.627G>A|p.Met209Ile |
S256 |
| 136920 | BAA10g22630 | A10 | 19378651 | C | T | downstream_gene_variant | MODIFIER | c.*97C>T| |
S153 |
| 136921 | BAA10g22640 | A10 | 19384009 | A | T | upstream_gene_variant | MODIFIER | c.-2098A>T| |
S26 |
| 136922 | BAA10g22640 | A10 | 19384076 | G | A | upstream_gene_variant | MODIFIER | c.-2031G>A| |
S287 |
| 136923 | BAA10g22650 | A10 | 19386451 | G | A | upstream_gene_variant | MODIFIER | c.-2151G>A| |
S216 |
| 136924 | BAA10g22650 | A10 | 19388004 | G | A | upstream_gene_variant | MODIFIER | c.-598G>A| |
S45 |
| 136925 | BAA10g22650 | A10 | 19388537 | G | A | upstream_gene_variant | MODIFIER | c.-65G>A| |
S164 |