| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164551 | BAA02g10980 | A02 | 4941089 | C | T | missense_variant | MODERATE | c.340C>T|p.Pro114Ser |
S292 |
| 164552 | BAA02g10980 | A02 | 4941963 | C | T | missense_variant | MODERATE | c.914C>T|p.Ser305Leu |
S209 |
| 164553 | BAA02g10980 | A02 | 4942229 | G | A | synonymous_variant | LOW | c.1071G>A|p.Gly357Gly |
S246 |
| 164554 | BAA02g10970 | A02 | 4943167 | G | A | downstream_gene_variant | MODIFIER | c.*4036G>A| |
S11 |
| 164555 | BAA02g10990 | A02 | 4943494 | C | T | synonymous_variant | LOW | c.2526G>A|p.Gly842Gly |
S186 |
| 164556 | BAA02g10990 | A02 | 4943529 | G | A | synonymous_variant | LOW | c.2491C>T|p.Leu831Leu |
S296 |
| 164557 | BAA02g10990 | A02 | 4943700 | G | A | missense_variant | MODERATE | c.2320C>T|p.Pro774Ser |
S223 |
| 164558 | BAA02g10990 | A02 | 4944696 | C | T | synonymous_variant | LOW | c.1617G>A|p.Gln539Gln |
S277 |
| 164559 | BAA02g10990 | A02 | 4945375 | G | A | synonymous_variant | LOW | c.1245C>T|p.Phe415Phe |
S264 |
| 164560 | BAA02g10990 | A02 | 4945504 | C | T | missense_variant | MODERATE | c.1116G>A|p.Met372Ile |
S263 |
| 164561 | BAA02g10990 | A02 | 4945984 | C | T | missense_variant | MODERATE | c.728G>A|p.Ser243Asn |
S100 |
| 164562 | BAA02g10990 | A02 | 4946450 | C | T | missense_variant | MODERATE | c.262G>A|p.Gly88Arg |
S172 S217 S275 |
| 164563 | BAA02g10990 | A02 | 4946505 | G | A | synonymous_variant | LOW | c.207C>T|p.Phe69Phe |
S228 |
| 164564 | BAA02g10990 | A02 | 4946610 | C | T | missense_variant&splice_region_variant | MODERATE | c.199G>A|p.Ala67Thr |
S144 |
| 164565 | BAA02g10990 | A02 | 4946728 | G | A | synonymous_variant | LOW | c.81C>T|p.Ala27Ala |
S247 |
| 164566 | BAA02g10990 | A02 | 4946810 | T | G | upstream_gene_variant | MODIFIER | c.-2A>C| |
S298 |
| 164567 | BAA02g10990 | A02 | 4946822 | G | A | upstream_gene_variant | MODIFIER | c.-14C>T| |
S308 |
| 164568 | BAA02g10990 | A02 | 4947541 | G | A | upstream_gene_variant | MODIFIER | c.-733C>T| |
S155 |
| 164569 | BAA02g10990 | A02 | 4948099 | T | A | upstream_gene_variant | MODIFIER | c.-1291A>T| |
S213 |
| 164570 | BAA02g10990 | A02 | 4948222 | G | A | upstream_gene_variant | MODIFIER | c.-1414C>T| |
S149 |
| 164571 | BAA02g10990 | A02 | 4948900 | C | T | upstream_gene_variant | MODIFIER | c.-2092G>A| |
S130 |
| 164572 | BAA02g10990 | A02 | 4949158 | A | G | upstream_gene_variant | MODIFIER | c.-2350T>C| |
S148 S30 S31 |
| 164573 | BAA02g10990 | A02 | 4949257 | T | A | upstream_gene_variant | MODIFIER | c.-2449A>T| |
S200 |
| 164574 | BAA02g10990 | A02 | 4949547 | G | A | upstream_gene_variant | MODIFIER | c.-2739C>T| |
S96 |
| 164575 | BAA02g10990 | A02 | 4950073 | G | A | upstream_gene_variant | MODIFIER | c.-3265C>T| |
S48 |