| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134301 | BAA10g20510 | A10 | 18425087 | C | T | upstream_gene_variant | MODIFIER | c.-2427C>T| |
S153 S213 |
| 134302 | BAA10g20500 | A10 | 18425937 | C | A | upstream_gene_variant | MODIFIER | c.-468G>T| |
S174 |
| 134303 | BAA10g20500 | A10 | 18426125 | C | G | upstream_gene_variant | MODIFIER | c.-656G>C| |
S123 |
| 134304 | BAA10g20500 | A10 | 18426491 | C | T | upstream_gene_variant | MODIFIER | c.-1022G>A| |
S195 |
| 134305 | BAA10g20500 | A10 | 18427333 | C | T | upstream_gene_variant | MODIFIER | c.-1864G>A| |
S183 |
| 134306 | BAA10g20510 | A10 | 18427660 | C | T | synonymous_variant | LOW | c.147C>T|p.Leu49Leu |
S83 S88 |
| 134307 | BAA10g20510 | A10 | 18428002 | C | T | synonymous_variant | LOW | c.489C>T|p.Ala163Ala |
S268 |
| 134308 | BAA10g20520 | A10 | 18430837 | G | A | missense_variant | MODERATE | c.1082G>A|p.Gly361Glu |
S111 |
| 134309 | BAA10g20540 | A10 | 18431422 | C | T | upstream_gene_variant | MODIFIER | c.-1453C>T| |
S87 |
| 134310 | BAA10g20540 | A10 | 18431558 | G | A | upstream_gene_variant | MODIFIER | c.-1317G>A| |
S79 S84 |
| 134311 | BAA10g20530 | A10 | 18431716 | G | A | missense_variant | MODERATE | c.572C>T|p.Ser191Phe |
S241 |
| 134312 | BAA10g20530 | A10 | 18432622 | G | A | upstream_gene_variant | MODIFIER | c.-103C>T| |
S270 |
| 134313 | BAA10g20530 | A10 | 18432762 | G | A | upstream_gene_variant | MODIFIER | c.-243C>T| |
S79 S84 |
| 134314 | BAA10g20540 | A10 | 18432938 | C | T | stop_gained | HIGH | c.64C>T|p.Arg22* |
S116 |
| 134315 | BAA10g20530 | A10 | 18435105 | G | A | upstream_gene_variant | MODIFIER | c.-2586C>T| |
S50 |
| 134316 | BAA10g20530 | A10 | 18435127 | G | A | upstream_gene_variant | MODIFIER | c.-2608C>T| |
S207 |
| 134317 | BAA10g20550 | A10 | 18435195 | C | T | missense_variant | MODERATE | c.50C>T|p.Thr17Met |
S211 S227 |
| 134318 | BAA10g20550 | A10 | 18437178 | C | T | missense_variant | MODERATE | c.1187C>T|p.Ser396Phe |
S113 |
| 134319 | BAA10g20560 | A10 | 18438514 | C | T | missense_variant | MODERATE | c.43C>T|p.Pro15Ser |
S76 |
| 134320 | BAA10g20570 | A10 | 18439198 | G | A | upstream_gene_variant | MODIFIER | c.-1695G>A| |
S138 |
| 134321 | BAA10g20570 | A10 | 18439856 | G | A | upstream_gene_variant | MODIFIER | c.-1037G>A| |
S3 |
| 134322 | BAA10g20570 | A10 | 18440050 | C | T | upstream_gene_variant | MODIFIER | c.-843C>T| |
S247 |
| 134323 | BAA10g20570 | A10 | 18440069 | G | A | upstream_gene_variant | MODIFIER | c.-824G>A| |
S50 |
| 134324 | BAA10g20570 | A10 | 18441378 | C | T | synonymous_variant | LOW | c.486C>T|p.Pro162Pro |
S133 |
| 134325 | BAA10g20570 | A10 | 18441706 | G | A | missense_variant | MODERATE | c.814G>A|p.Glu272Lys |
S50 |