| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 122251 | BAA10g12650 | A10 | 14053451 | G | A | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S74 |
| 122252 | BAA10g12650 | A10 | 14053755 | C | T | upstream_gene_variant | MODIFIER | c.-2888C>T| |
S25 |
| 122253 | BAA10g12650 | A10 | 14055141 | T | A | upstream_gene_variant | MODIFIER | c.-1502T>A| |
S125 |
| 122254 | BAA10g12650 | A10 | 14055463 | G | A | upstream_gene_variant | MODIFIER | c.-1180G>A| |
S267 |
| 122255 | BAA10g12650 | A10 | 14056309 | G | A | upstream_gene_variant | MODIFIER | c.-334G>A| |
S55 |
| 122256 | BAA10g12650 | A10 | 14056473 | G | A | upstream_gene_variant | MODIFIER | c.-170G>A| |
S57 |
| 122257 | BAA10g12650 | A10 | 14056765 | G | A | synonymous_variant | LOW | c.123G>A|p.Thr41Thr |
S75 S81 |
| 122258 | BAA10g12650 | A10 | 14056817 | C | T | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S167 |
| 122259 | BAA10g12650 | A10 | 14056966 | C | T | synonymous_variant | LOW | c.324C>T|p.Asn108Asn |
S243 S299 |
| 122260 | BAA10g12660 | A10 | 14058147 | C | T | downstream_gene_variant | MODIFIER | c.*2069G>A| |
S28 |
| 122261 | BAA10g12660 | A10 | 14058504 | C | T | downstream_gene_variant | MODIFIER | c.*1712G>A| |
S42 |
| 122262 | BAA10g12650 | A10 | 14058631 | G | A | downstream_gene_variant | MODIFIER | c.*9G>A| |
S90 |
| 122263 | BAA10g12670 | A10 | 14061575 | G | A | upstream_gene_variant | MODIFIER | c.-2233G>A| |
S160 |
| 122264 | BAA10g12670 | A10 | 14061594 | C | T | upstream_gene_variant | MODIFIER | c.-2214C>T| |
S211 S227 |
| 122265 | BAA10g12670 | A10 | 14061638 | C | T | upstream_gene_variant | MODIFIER | c.-2170C>T| |
S260 |
| 122266 | BAA10g12660 | A10 | 14061826 | G | A | synonymous_variant | LOW | c.228C>T|p.Phe76Phe |
S241 |
| 122267 | BAA10g12660 | A10 | 14062825 | G | A | upstream_gene_variant | MODIFIER | c.-772C>T| |
S209 |
| 122268 | BAA10g12660 | A10 | 14062846 | G | A | upstream_gene_variant | MODIFIER | c.-793C>T| |
S261 |
| 122269 | BAA10g12660 | A10 | 14062956 | C | T | upstream_gene_variant | MODIFIER | c.-903G>A| |
S121 |
| 122270 | BAA10g12660 | A10 | 14063088 | C | T | upstream_gene_variant | MODIFIER | c.-1035G>A| |
S25 |
| 122271 | BAA10g12660 | A10 | 14063343 | G | A | upstream_gene_variant | MODIFIER | c.-1290C>T| |
S129 |
| 122272 | BAA10g12660 | A10 | 14064134 | C | T | upstream_gene_variant | MODIFIER | c.-2081G>A| |
S140 |
| 122273 | BAA10g12660 | A10 | 14066359 | G | A | upstream_gene_variant | MODIFIER | c.-4306C>T| |
S48 |
| 122274 | BAA10g12660 | A10 | 14066400 | C | T | upstream_gene_variant | MODIFIER | c.-4347G>A| |
S149 |
| 122275 | BAA10g12660 | A10 | 14066810 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S183 |