| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 176551 | BAA02g18410 | A02 | 9403172 | G | A | upstream_gene_variant | MODIFIER | c.-352C>T| |
S98 |
| 176552 | BAA02g18410 | A02 | 9403183 | G | A | upstream_gene_variant | MODIFIER | c.-363C>T| |
S95 |
| 176553 | BAA02g18410 | A02 | 9403373 | G | A | upstream_gene_variant | MODIFIER | c.-553C>T| |
S166 |
| 176554 | BAA02g18420 | A02 | 9403694 | C | T | synonymous_variant | LOW | c.1518G>A|p.Arg506Arg |
S224 |
| 176555 | BAA02g18420 | A02 | 9404086 | C | T | missense_variant | MODERATE | c.1126G>A|p.Asp376Asn |
S245 |
| 176556 | BAA02g18420 | A02 | 9404231 | G | A | synonymous_variant | LOW | c.981C>T|p.Phe327Phe |
S47 S48 |
| 176557 | BAA02g18420 | A02 | 9404277 | C | T | missense_variant | MODERATE | c.935G>A|p.Ser312Asn |
S135 |
| 176558 | BAA02g18420 | A02 | 9405238 | C | T | synonymous_variant | LOW | c.789G>A|p.Lys263Lys |
S119 |
| 176559 | BAA02g18410 | A02 | 9406202 | C | T | upstream_gene_variant | MODIFIER | c.-3382G>A| |
S142 |
| 176560 | BAA02g18410 | A02 | 9406286 | C | T | upstream_gene_variant | MODIFIER | c.-3466G>A| |
S218 |
| 176561 | BAA02g18430 | A02 | 9407535 | G | A | missense_variant | MODERATE | c.131C>T|p.Pro44Leu |
S190 |
| 176562 | BAA02g18440 | A02 | 9407770 | A | C | missense_variant | MODERATE | c.622T>G|p.Ser208Ala |
S5 |
| 176563 | BAA02g18440 | A02 | 9407780 | G | A | synonymous_variant | LOW | c.612C>T|p.Cys204Cys |
S5 |
| 176564 | BAA02g18440 | A02 | 9407789 | G | A | synonymous_variant | LOW | c.603C>T|p.Asp201Asp |
S5 |
| 176565 | BAA02g18440 | A02 | 9407803 | C | T | missense_variant | MODERATE | c.589G>A|p.Val197Ile |
S5 |
| 176566 | BAA02g18440 | A02 | 9407807 | A | T | missense_variant | MODERATE | c.585T>A|p.His195Gln |
S5 |
| 176567 | BAA02g18440 | A02 | 9407887 | C | T | missense_variant | MODERATE | c.505G>A|p.Ala169Thr |
S163 |
| 176568 | BAA02g18440 | A02 | 9408092 | G | A | synonymous_variant | LOW | c.300C>T|p.Asp100Asp |
S136 |
| 176569 | BAA02g18440 | A02 | 9408268 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S242 |
| 176570 | BAA02g18420 | A02 | 9408795 | G | A | upstream_gene_variant | MODIFIER | c.-2769C>T| |
S20 |
| 176571 | BAA02g18420 | A02 | 9409442 | C | T | upstream_gene_variant | MODIFIER | c.-3416G>A| |
S186 |
| 176572 | BAA02g18420 | A02 | 9409531 | C | T | upstream_gene_variant | MODIFIER | c.-3505G>A| |
S178 |
| 176573 | BAA02g18420 | A02 | 9409854 | G | A | upstream_gene_variant | MODIFIER | c.-3828C>T| |
S150 |
| 176574 | BAA02g18420 | A02 | 9410102 | C | T | upstream_gene_variant | MODIFIER | c.-4076G>A| |
S71 |
| 176575 | BAA02g18430 | A02 | 9411258 | C | T | upstream_gene_variant | MODIFIER | c.-3593G>A| |
S75 S81 |