| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 114351 | BAA10g09270 | A10 | 11272596 | A | T | upstream_gene_variant | MODIFIER | c.-3670T>A| |
S237 |
| 114352 | BAA10g09270 | A10 | 11272610 | C | T | upstream_gene_variant | MODIFIER | c.-3684G>A| |
S287 |
| 114353 | BAA10g09270 | A10 | 11273108 | G | A | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S135 S185 S273 S68 |
| 114354 | BAA10g09280 | A10 | 11274698 | G | A | downstream_gene_variant | MODIFIER | c.*1256C>T| |
S178 |
| 114355 | BAA10g09280 | A10 | 11275482 | G | A | downstream_gene_variant | MODIFIER | c.*472C>T| |
S4 |
| 114356 | BAA10g09280 | A10 | 11276243 | C | T | missense_variant | MODERATE | c.1717G>A|p.Ala573Thr |
S177 |
| 114357 | BAA10g09280 | A10 | 11276400 | T | G | intron_variant | MODIFIER | c.1709+61A>C| |
S15 S3 |
| 114358 | BAA10g09280 | A10 | 11277199 | C | T | missense_variant | MODERATE | c.1486G>A|p.Glu496Lys |
S194 |
| 114359 | BAA10g09280 | A10 | 11277633 | G | A | intron_variant | MODIFIER | c.1173-37C>T| |
S279 |
| 114360 | BAA10g09280 | A10 | 11278447 | G | A | missense_variant | MODERATE | c.962C>T|p.Thr321Ile |
S138 |
| 114361 | BAA10g09280 | A10 | 11278548 | A | T | splice_region_variant&intron_variant | LOW | c.958+5T>A| |
S15 |
| 114362 | BAA10g09280 | A10 | 11278889 | C | T | missense_variant | MODERATE | c.817G>A|p.Gly273Arg |
S38 |
| 114363 | BAA10g09280 | A10 | 11279544 | C | T | intron_variant | MODIFIER | c.568+73G>A| |
S286 |
| 114364 | BAA10g09280 | A10 | 11280233 | T | G | missense_variant | MODERATE | c.236A>C|p.Lys79Thr |
S15 S3 |
| 114365 | BAA10g09280 | A10 | 11280467 | C | T | missense_variant | MODERATE | c.94G>A|p.Glu32Lys |
S162 |
| 114366 | BAA10g09280 | A10 | 11280895 | C | T | upstream_gene_variant | MODIFIER | c.-200G>A| |
S270 |
| 114367 | BAA10g09290 | A10 | 11285131 | C | T | missense_variant | MODERATE | c.725G>A|p.Ser242Asn |
S28 |
| 114368 | BAA10g09290 | A10 | 11285680 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Phe |
S65 |
| 114369 | BAA10g09290 | A10 | 11285779 | G | A | missense_variant | MODERATE | c.224C>T|p.Ala75Val |
S274 |
| 114370 | BAA10g09290 | A10 | 11285944 | G | A | missense_variant | MODERATE | c.59C>T|p.Ala20Val |
S226 |
| 114371 | BAA10g09290 | A10 | 11285950 | G | A | missense_variant | MODERATE | c.53C>T|p.Ser18Phe |
S192 S291 |
| 114372 | BAA10g09290 | A10 | 11286102 | G | A | upstream_gene_variant | MODIFIER | c.-100C>T| |
S107 |
| 114373 | BAA10g09290 | A10 | 11286154 | G | A | upstream_gene_variant | MODIFIER | c.-152C>T| |
S209 |
| 114374 | BAA10g09290 | A10 | 11286283 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S308 |
| 114375 | BAA10g09290 | A10 | 11286668 | G | A | upstream_gene_variant | MODIFIER | c.-666C>T| |
S32 |