| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 92351 | BAA10g02110 | A10 | 988236 | G | A | upstream_gene_variant | MODIFIER | c.-3176G>A| |
S124 |
| 92352 | BAA10g02110 | A10 | 988359 | G | A | upstream_gene_variant | MODIFIER | c.-3053G>A| |
S290 |
| 92353 | BAA10g02110 | A10 | 989032 | G | A | upstream_gene_variant | MODIFIER | c.-2380G>A| |
S164 |
| 92354 | BAA10g02110 | A10 | 989576 | C | T | upstream_gene_variant | MODIFIER | c.-1836C>T| |
S195 |
| 92355 | BAA10g02110 | A10 | 991219 | G | A | upstream_gene_variant | MODIFIER | c.-193G>A| |
S296 |
| 92356 | BAA10g02110 | A10 | 991411 | G | A | upstream_gene_variant | MODIFIER | c.-1G>A| |
S156 |
| 92357 | BAA10g02110 | A10 | 991567 | C | T | synonymous_variant | LOW | c.156C>T|p.Ser52Ser |
S224 |
| 92358 | BAA10g02110 | A10 | 992177 | G | A | missense_variant | MODERATE | c.412G>A|p.Val138Ile |
S62 |
| 92359 | BAA10g02110 | A10 | 992641 | G | A | missense_variant | MODERATE | c.670G>A|p.Glu224Lys |
S292 |
| 92360 | BAA10g02110 | A10 | 992664 | C | T | synonymous_variant | LOW | c.693C>T|p.Thr231Thr |
S11 |
| 92361 | BAA10g02110 | A10 | 992802 | G | A | synonymous_variant | LOW | c.831G>A|p.Gln277Gln |
S242 |
| 92362 | BAA10g02110 | A10 | 994225 | C | T | missense_variant | MODERATE | c.1937C>T|p.Pro646Leu |
S143 |
| 92363 | BAA10g02110 | A10 | 994914 | G | A | synonymous_variant | LOW | c.2358G>A|p.Lys786Lys |
S215 |
| 92364 | BAA10g02120 | A10 | 995065 | G | A | downstream_gene_variant | MODIFIER | c.*968C>T| |
S18 |
| 92365 | BAA10g02110 | A10 | 995387 | G | A | missense_variant | MODERATE | c.2725G>A|p.Glu909Lys |
S45 |
| 92366 | BAA10g02110 | A10 | 995658 | C | T | downstream_gene_variant | MODIFIER | c.*116C>T| |
S165 |
| 92367 | BAA10g02120 | A10 | 996767 | G | A | missense_variant | MODERATE | c.658C>T|p.Pro220Ser |
S126 |
| 92368 | BAA10g02120 | A10 | 996852 | C | T | synonymous_variant | LOW | c.573G>A|p.Gln191Gln |
S297 |
| 92369 | BAA10g02120 | A10 | 997074 | C | T | synonymous_variant | LOW | c.351G>A|p.Leu117Leu |
S35 |
| 92370 | BAA10g02120 | A10 | 997781 | G | A | upstream_gene_variant | MODIFIER | c.-357C>T| |
S176 S303 |
| 92371 | BAA10g02120 | A10 | 999409 | G | A | upstream_gene_variant | MODIFIER | c.-1985C>T| |
S176 |
| 92372 | BAA10g02120 | A10 | 999640 | C | T | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S270 |
| 92373 | BAA10g02120 | A10 | 1000857 | C | T | upstream_gene_variant | MODIFIER | c.-3433G>A| |
S11 |
| 92374 | BAA10g02120 | A10 | 1001161 | G | A | upstream_gene_variant | MODIFIER | c.-3737C>T| |
S20 |
| 92375 | BAA10g02120 | A10 | 1001980 | G | A | upstream_gene_variant | MODIFIER | c.-4556C>T| |
S216 |