| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 84951 | BAA01g45010 | A01 | 30031441 | C | T | upstream_gene_variant | MODIFIER | c.-814G>A| |
S256 |
| 84952 | BAA01g45020 | A01 | 30032141 | G | A | missense_variant | MODERATE | c.212G>A|p.Arg71His |
S244 |
| 84953 | BAA01g45020 | A01 | 30032792 | G | T | missense_variant | MODERATE | c.797G>T|p.Trp266Leu |
S94 |
| 84954 | BAA01g45010 | A01 | 30032878 | C | T | upstream_gene_variant | MODIFIER | c.-2251G>A| |
S289 S290 |
| 84955 | BAA01g45010 | A01 | 30032976 | G | A | upstream_gene_variant | MODIFIER | c.-2349C>T| |
S274 |
| 84956 | BAA01g45030 | A01 | 30033125 | C | T | stop_gained | HIGH | c.91C>T|p.Gln31* |
S85 |
| 84957 | BAA01g45030 | A01 | 30033216 | G | A | splice_region_variant&intron_variant | LOW | c.178+4G>A| |
S151 |
| 84958 | BAA01g45010 | A01 | 30033262 | G | A | upstream_gene_variant | MODIFIER | c.-2635C>T| |
S223 |
| 84959 | BAA01g45010 | A01 | 30033296 | C | T | upstream_gene_variant | MODIFIER | c.-2669G>A| |
S133 |
| 84960 | BAA01g45030 | A01 | 30034414 | G | A | synonymous_variant | LOW | c.888G>A|p.Lys296Lys |
S262 |
| 84961 | BAA01g45030 | A01 | 30034523 | G | A | missense_variant | MODERATE | c.997G>A|p.Gly333Arg |
S217 |
| 84962 | BAA01g45010 | A01 | 30035370 | T | A | upstream_gene_variant | MODIFIER | c.-4743A>T| |
S197 |
| 84963 | BAA01g45040 | A01 | 30035782 | G | A | missense_variant | MODERATE | c.107G>A|p.Gly36Glu |
S298 |
| 84964 | BAA01g45040 | A01 | 30036433 | C | T | synonymous_variant | LOW | c.633C>T|p.Arg211Arg |
S233 S239 |
| 84965 | BAA01g45040 | A01 | 30036473 | C | T | missense_variant | MODERATE | c.673C>T|p.Arg225Trp |
S35 |
| 84966 | BAA01g45040 | A01 | 30036509 | G | A | missense_variant | MODERATE | c.709G>A|p.Val237Met |
S143 |
| 84967 | BAA01g45040 | A01 | 30037009 | G | A | synonymous_variant | LOW | c.1119G>A|p.Lys373Lys |
S114 S119 S123 S256 |
| 84968 | BAA01g45040 | A01 | 30037020 | G | A | missense_variant&splice_region_variant | MODERATE | c.1130G>A|p.Arg377His |
S284 |
| 84969 | BAA01g45040 | A01 | 30037085 | G | A | splice_region_variant&intron_variant | LOW | c.1133-4G>A| |
S257 |
| 84970 | BAA01g45040 | A01 | 30037554 | G | A | synonymous_variant | LOW | c.1536G>A|p.Arg512Arg |
S86 |
| 84971 | BAA01g45040 | A01 | 30037672 | G | A | missense_variant | MODERATE | c.1654G>A|p.Glu552Lys |
S271 |
| 84972 | BAA01g45030 | A01 | 30038474 | G | A | downstream_gene_variant | MODIFIER | c.*3694G>A| |
S70 |
| 84973 | BAA01g45030 | A01 | 30039396 | G | A | downstream_gene_variant | MODIFIER | c.*4616G>A| |
S103 |
| 84974 | BAA01g45040 | A01 | 30039436 | G | A | missense_variant | MODERATE | c.2924G>A|p.Arg975Lys |
S116 |
| 84975 | BAA01g45040 | A01 | 30039488 | G | A | stop_gained | HIGH | c.2976G>A|p.Trp992* |
S135 S68 |