| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151501 | BAA02g00200 | A02 | 133167 | G | A | synonymous_variant | LOW | c.225C>T|p.Pro75Pro |
S87 |
| 151502 | BAA02g00190 | A02 | 133492 | C | T | upstream_gene_variant | MODIFIER | c.-2227G>A| |
S16 |
| 151503 | BAA02g00210 | A02 | 134498 | C | T | splice_region_variant&intron_variant | LOW | c.302+5C>T| |
S278 |
| 151504 | BAA02g00190 | A02 | 135084 | G | A | upstream_gene_variant | MODIFIER | c.-3819C>T| |
S131 |
| 151505 | BAA02g00190 | A02 | 135248 | G | A | upstream_gene_variant | MODIFIER | c.-3983C>T| |
S26 |
| 151506 | BAA02g00220 | A02 | 135590 | C | T | missense_variant | MODERATE | c.146C>T|p.Ser49Phe |
S301 S304 |
| 151507 | BAA02g00200 | A02 | 136963 | C | T | upstream_gene_variant | MODIFIER | c.-3572G>A| |
S19 |
| 151508 | BAA02g00200 | A02 | 137183 | C | T | upstream_gene_variant | MODIFIER | c.-3792G>A| |
S118 |
| 151509 | BAA02g00200 | A02 | 137448 | G | A | upstream_gene_variant | MODIFIER | c.-4057C>T| |
S236 |
| 151510 | BAA02g00200 | A02 | 137633 | C | T | upstream_gene_variant | MODIFIER | c.-4242G>A| |
S245 |
| 151511 | BAA02g00230 | A02 | 137954 | C | T | synonymous_variant | LOW | c.99C>T|p.Leu33Leu |
S75 S81 |
| 151512 | BAA02g00230 | A02 | 138314 | G | A | synonymous_variant | LOW | c.459G>A|p.Arg153Arg |
S202 |
| 151513 | BAA02g00240 | A02 | 138977 | C | T | upstream_gene_variant | MODIFIER | c.-842C>T| |
S155 S211 |
| 151514 | BAA02g00240 | A02 | 139916 | C | T | missense_variant | MODERATE | c.98C>T|p.Pro33Leu |
S221 |
| 151515 | BAA02g00240 | A02 | 139967 | C | T | missense_variant | MODERATE | c.149C>T|p.Ser50Phe |
S82 S92 |
| 151516 | BAA02g00240 | A02 | 140744 | C | T | synonymous_variant | LOW | c.562C>T|p.Leu188Leu |
S177 |
| 151517 | BAA02g00220 | A02 | 141333 | C | T | downstream_gene_variant | MODIFIER | c.*4812C>T| |
S255 |
| 151518 | BAA02g00240 | A02 | 142267 | G | A | missense_variant | MODERATE | c.1214G>A|p.Ser405Asn |
S206 S26 |
| 151519 | BAA02g00240 | A02 | 142401 | G | A | missense_variant | MODERATE | c.1348G>A|p.Gly450Arg |
S249 |
| 151520 | BAA02g00240 | A02 | 142548 | G | A | missense_variant | MODERATE | c.1495G>A|p.Asp499Asn |
S153 S213 |
| 151521 | BAA02g00240 | A02 | 143932 | G | A | intron_variant | MODIFIER | c.2245-131G>A| |
S165 |
| 151522 | BAA02g00240 | A02 | 144189 | C | T | intron_variant | MODIFIER | c.2361+10C>T| |
S56 |
| 151523 | BAA02g00250 | A02 | 145184 | C | T | upstream_gene_variant | MODIFIER | c.-4313C>T| |
S270 |
| 151524 | BAA02g00240 | A02 | 145434 | C | T | missense_variant | MODERATE | c.2971C>T|p.Pro991Ser |
S82 S92 |
| 151525 | BAA02g00240 | A02 | 145508 | G | A | synonymous_variant | LOW | c.3045G>A|p.Glu1015Glu |
S173 |