| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 160301 | BAA02g07540 | A02 | 3237552 | C | T | missense_variant | MODERATE | c.4711G>A|p.Val1571Met |
S15 S3 |
| 160302 | BAA02g07540 | A02 | 3238517 | G | A | synonymous_variant | LOW | c.3970C>T|p.Leu1324Leu |
S59 |
| 160303 | BAA02g07540 | A02 | 3238693 | C | T | intron_variant | MODIFIER | c.3844-50G>A| |
S171 |
| 160304 | BAA02g07540 | A02 | 3238939 | G | A | missense_variant | MODERATE | c.3764C>T|p.Ser1255Leu |
S133 |
| 160305 | BAA02g07540 | A02 | 3241730 | T | C | intron_variant | MODIFIER | c.2630+191A>G| |
S157 S166 S167 S236 S262 S263 |
| 160306 | BAA02g07540 | A02 | 3241985 | G | A | missense_variant | MODERATE | c.2566C>T|p.Leu856Phe |
S296 |
| 160307 | BAA02g07540 | A02 | 3242563 | C | T | intron_variant | MODIFIER | c.2249-171G>A| |
S192 |
| 160308 | BAA02g07540 | A02 | 3244034 | C | T | intron_variant | MODIFIER | c.1670-262G>A| |
S250 |
| 160309 | BAA02g07540 | A02 | 3244604 | C | T | intron_variant | MODIFIER | c.1669+107G>A| |
S32 |
| 160310 | BAA02g07540 | A02 | 3244643 | C | T | intron_variant | MODIFIER | c.1669+68G>A| |
S56 |
| 160311 | BAA02g07540 | A02 | 3244879 | G | A | missense_variant | MODERATE | c.1501C>T|p.Pro501Ser |
S125 |
| 160312 | BAA02g07540 | A02 | 3244947 | G | A | missense_variant | MODERATE | c.1433C>T|p.Ala478Val |
S23 |
| 160313 | BAA02g07540 | A02 | 3244984 | G | A | missense_variant | MODERATE | c.1396C>T|p.Pro466Ser |
S59 |
| 160314 | BAA02g07540 | A02 | 3245687 | G | A | missense_variant | MODERATE | c.911C>T|p.Ser304Phe |
S205 |
| 160315 | BAA02g07540 | A02 | 3246937 | C | T | missense_variant | MODERATE | c.371G>A|p.Gly124Glu |
S277 |
| 160316 | BAA02g07540 | A02 | 3249000 | C | T | upstream_gene_variant | MODIFIER | c.-1250G>A| |
S152 |
| 160317 | BAA02g07540 | A02 | 3249233 | G | A | upstream_gene_variant | MODIFIER | c.-1483C>T| |
S197 |
| 160318 | BAA02g07540 | A02 | 3251072 | G | A | upstream_gene_variant | MODIFIER | c.-3322C>T| |
S190 |
| 160319 | BAA02g07540 | A02 | 3251327 | G | A | upstream_gene_variant | MODIFIER | c.-3577C>T| |
S136 |
| 160320 | BAA02g07550 | A02 | 3251646 | C | T | missense_variant | MODERATE | c.310C>T|p.Arg104Cys |
S66 |
| 160321 | BAA02g07540 | A02 | 3252503 | G | A | upstream_gene_variant | MODIFIER | c.-4753C>T| |
S139 |
| 160322 | BAA02g07550 | A02 | 3253762 | G | A | missense_variant | MODERATE | c.1052G>A|p.Arg351Lys |
S96 |
| 160323 | BAA02g07560 | A02 | 3254532 | C | T | upstream_gene_variant | MODIFIER | c.-1233C>T| |
S181 |
| 160324 | BAA02g07560 | A02 | 3254715 | A | G | upstream_gene_variant | MODIFIER | c.-1050A>G| |
S34 |
| 160325 | BAA02g07560 | A02 | 3254849 | C | T | upstream_gene_variant | MODIFIER | c.-916C>T| |
S94 |