| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 97301 | BAA10g05190 | A10 | 2690908 | C | T | upstream_gene_variant | MODIFIER | c.-3126C>T| |
S246 |
| 97302 | BAA10g05190 | A10 | 2691150 | G | A | upstream_gene_variant | MODIFIER | c.-2884G>A| |
S97 |
| 97303 | BAA10g05180 | A10 | 2693036 | C | T | upstream_gene_variant | MODIFIER | c.-387G>A| |
S193 |
| 97304 | BAA10g05180 | A10 | 2695667 | G | T | upstream_gene_variant | MODIFIER | c.-3018C>A| |
S135 S152 S185 S203 |
| 97305 | BAA10g05190 | A10 | 2698070 | G | A | downstream_gene_variant | MODIFIER | c.*3421G>A| |
S167 |
| 97306 | BAA10g05190 | A10 | 2699031 | C | T | downstream_gene_variant | MODIFIER | c.*4382C>T| |
S265 |
| 97307 | BAA10g05200-BAA10g05210 | A10 | 2700634 | C | T | intergenic_region | MODIFIER | n.2700634C>T| |
S121 |
| 97308 | BAA10g05200-BAA10g05210 | A10 | 2700797 | C | T | intergenic_region | MODIFIER | n.2700797C>T| |
S155 S211 |
| 97309 | BAA10g05200-BAA10g05210 | A10 | 2701740 | G | A | intergenic_region | MODIFIER | n.2701740G>A| |
S172 S217 |
| 97310 | BAA10g05210 | A10 | 2706781 | C | T | upstream_gene_variant | MODIFIER | c.-4674C>T| |
S42 |
| 97311 | BAA10g05210 | A10 | 2707472 | G | A | upstream_gene_variant | MODIFIER | c.-3983G>A| |
S184 |
| 97312 | BAA10g05210 | A10 | 2708806 | C | T | upstream_gene_variant | MODIFIER | c.-2649C>T| |
S165 |
| 97313 | BAA10g05210 | A10 | 2708864 | C | T | upstream_gene_variant | MODIFIER | c.-2591C>T| |
S187 |
| 97314 | BAA10g05210 | A10 | 2711107 | G | A | upstream_gene_variant | MODIFIER | c.-348G>A| |
S167 |
| 97315 | BAA10g05210 | A10 | 2711516 | C | T | missense_variant | MODERATE | c.62C>T|p.Ser21Phe |
S226 |
| 97316 | BAA10g05210 | A10 | 2711744 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Leu |
S63 |
| 97317 | BAA10g05220 | A10 | 2712460 | C | T | missense_variant | MODERATE | c.44C>T|p.Thr15Ile |
S186 |
| 97318 | BAA10g05220 | A10 | 2712966 | G | A | missense_variant | MODERATE | c.550G>A|p.Asp184Asn |
S95 |
| 97319 | BAA10g05250 | A10 | 2714444 | G | A | upstream_gene_variant | MODIFIER | c.-274G>A| |
S176 |
| 97320 | BAA10g05250 | A10 | 2715324 | G | A | missense_variant | MODERATE | c.607G>A|p.Glu203Lys |
S11 |
| 97321 | BAA10g05270 | A10 | 2715566 | G | A | upstream_gene_variant | MODIFIER | c.-3237G>A| |
S167 |
| 97322 | BAA10g05260 | A10 | 2716680 | C | T | missense_variant | MODERATE | c.1286G>A|p.Gly429Glu |
S272 |
| 97323 | BAA10g05260 | A10 | 2716928 | C | T | missense_variant | MODERATE | c.1120G>A|p.Ala374Thr |
S292 |
| 97324 | BAA10g05260 | A10 | 2717630 | G | A | synonymous_variant | LOW | c.418C>T|p.Leu140Leu |
S241 |
| 97325 | BAA10g05260 | A10 | 2717906 | C | T | missense_variant | MODERATE | c.142G>A|p.Asp48Asn |
S119 |