| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131001 | BAA10g18420 | A10 | 17241585 | C | T | upstream_gene_variant | MODIFIER | c.-1004G>A| |
S249 |
| 131002 | BAA10g18420 | A10 | 17242954 | G | A | upstream_gene_variant | MODIFIER | c.-2373C>T| |
S262 |
| 131003 | BAA10g18420 | A10 | 17243102 | G | A | upstream_gene_variant | MODIFIER | c.-2521C>T| |
S130 |
| 131004 | BAA10g18420 | A10 | 17244162 | C | T | upstream_gene_variant | MODIFIER | c.-3581G>A| |
S47 |
| 131005 | BAA10g18440 | A10 | 17248561 | G | A | upstream_gene_variant | MODIFIER | c.-2113G>A| |
S148 S210 |
| 131006 | BAA10g18440 | A10 | 17248918 | G | A | upstream_gene_variant | MODIFIER | c.-1756G>A| |
S288 |
| 131007 | BAA10g18440 | A10 | 17249298 | C | T | upstream_gene_variant | MODIFIER | c.-1376C>T| |
S195 |
| 131008 | BAA10g18440 | A10 | 17250529 | G | A | upstream_gene_variant | MODIFIER | c.-145G>A| |
S74 |
| 131009 | BAA10g18430 | A10 | 17251020 | G | A | downstream_gene_variant | MODIFIER | c.*405G>A| |
S184 |
| 131010 | BAA10g18430 | A10 | 17251868 | C | T | downstream_gene_variant | MODIFIER | c.*1253C>T| |
S25 |
| 131011 | BAA10g18430 | A10 | 17251986 | G | A | downstream_gene_variant | MODIFIER | c.*1371G>A| |
S150 |
| 131012 | BAA10g18450 | A10 | 17252946 | C | T | missense_variant | MODERATE | c.1363G>A|p.Asp455Asn |
S260 |
| 131013 | BAA10g18450 | A10 | 17254095 | G | A | synonymous_variant | LOW | c.768C>T|p.Phe256Phe |
S32 |
| 131014 | BAA10g18450 | A10 | 17257714 | C | T | upstream_gene_variant | MODIFIER | c.-2600G>A| |
S160 |
| 131015 | BAA10g18470 | A10 | 17258682 | C | T | missense_variant | MODERATE | c.169G>A|p.Gly57Arg |
S186 |
| 131016 | BAA10g18450 | A10 | 17258926 | C | T | upstream_gene_variant | MODIFIER | c.-3812G>A| |
S20 |
| 131017 | BAA10g18450 | A10 | 17259184 | C | T | upstream_gene_variant | MODIFIER | c.-4070G>A| |
S211 |
| 131018 | BAA10g18480 | A10 | 17266215 | C | T | downstream_gene_variant | MODIFIER | c.*1579G>A| |
S108 |
| 131019 | BAA10g18480 | A10 | 17267908 | C | T | synonymous_variant | LOW | c.387G>A|p.Thr129Thr |
S244 |
| 131020 | BAA10g18480 | A10 | 17267944 | C | T | missense_variant | MODERATE | c.351G>A|p.Met117Ile |
S305 |
| 131021 | BAA10g18480 | A10 | 17268423 | C | T | upstream_gene_variant | MODIFIER | c.-129G>A| |
S68 |
| 131022 | BAA10g18480 | A10 | 17269380 | C | T | upstream_gene_variant | MODIFIER | c.-1086G>A| |
S305 |
| 131023 | BAA10g18480 | A10 | 17272881 | C | T | upstream_gene_variant | MODIFIER | c.-4587G>A| |
S146 |
| 131024 | BAA10g18480 | A10 | 17273289 | G | A | upstream_gene_variant | MODIFIER | c.-4995C>T| |
S129 |
| 131025 | BAA10g18480-BAA10g18490 | A10 | 17273597 | C | T | intergenic_region | MODIFIER | n.17273597C>T| |
S20 |