| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151551 | BAA02g00240 | A02 | 146130 | G | A | missense_variant&splice_region_variant | MODERATE | c.3268G>A|p.Gly1090Arg |
S223 |
| 151552 | BAA02g00240 | A02 | 146203 | G | A | missense_variant | MODERATE | c.3341G>A|p.Arg1114Lys |
S266 |
| 151553 | BAA02g00250 | A02 | 146273 | G | A | upstream_gene_variant | MODIFIER | c.-3224G>A| |
S206 S26 |
| 151554 | BAA02g00240 | A02 | 147711 | G | A | missense_variant | MODERATE | c.4189G>A|p.Val1397Met |
S72 S78 |
| 151555 | BAA02g00250 | A02 | 147997 | G | A | upstream_gene_variant | MODIFIER | c.-1500G>A| |
S90 |
| 151556 | BAA02g00250 | A02 | 148556 | C | A | upstream_gene_variant | MODIFIER | c.-941C>A| |
S182 |
| 151557 | BAA02g00250 | A02 | 149293 | G | A | upstream_gene_variant | MODIFIER | c.-204G>A| |
S20 |
| 151558 | BAA02g00250 | A02 | 149669 | G | A | missense_variant | MODERATE | c.173G>A|p.Arg58Lys |
S60 |
| 151559 | BAA02g00250 | A02 | 150777 | G | A | missense_variant | MODERATE | c.569G>A|p.Ser190Asn |
S128 |
| 151560 | BAA02g00250 | A02 | 151019 | G | A | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S302 |
| 151561 | BAA02g00250 | A02 | 151028 | G | A | missense_variant | MODERATE | c.820G>A|p.Asp274Asn |
S189 |
| 151562 | BAA02g00260 | A02 | 152668 | C | T | missense_variant | MODERATE | c.1207G>A|p.Asp403Asn |
S40 S49 |
| 151563 | BAA02g00260 | A02 | 152791 | C | T | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S167 |
| 151564 | BAA02g00260 | A02 | 152928 | C | T | missense_variant&splice_region_variant | MODERATE | c.947G>A|p.Gly316Glu |
S47 |
| 151565 | BAA02g00260 | A02 | 155543 | C | T | upstream_gene_variant | MODIFIER | c.-1163G>A| |
S172 S217 |
| 151566 | BAA02g00260 | A02 | 155550 | G | A | upstream_gene_variant | MODIFIER | c.-1170C>T| |
S165 |
| 151567 | BAA02g00260 | A02 | 155560 | C | T | upstream_gene_variant | MODIFIER | c.-1180G>A| |
S181 |
| 151568 | BAA02g00260 | A02 | 156529 | C | T | upstream_gene_variant | MODIFIER | c.-2149G>A| |
S180 |
| 151569 | BAA02g00260 | A02 | 157141 | C | T | upstream_gene_variant | MODIFIER | c.-2761G>A| |
S274 |
| 151570 | BAA02g00260 | A02 | 157625 | C | T | upstream_gene_variant | MODIFIER | c.-3245G>A| |
S19 |
| 151571 | BAA02g00280 | A02 | 160625 | G | A | upstream_gene_variant | MODIFIER | c.-4480G>A| |
S25 |
| 151572 | BAA02g00280 | A02 | 162502 | C | T | upstream_gene_variant | MODIFIER | c.-2603C>T| |
S6 |
| 151573 | BAA02g00280 | A02 | 163027 | G | A | upstream_gene_variant | MODIFIER | c.-2078G>A| |
S51 |
| 151574 | BAA02g00280 | A02 | 164337 | C | T | upstream_gene_variant | MODIFIER | c.-768C>T| |
S167 |
| 151575 | BAA02g00280 | A02 | 165156 | G | A | missense_variant | MODERATE | c.52G>A|p.Val18Ile |
S265 |