| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 28601 | BAA01g20220 | A01 | 9942730 | C | T | upstream_gene_variant | MODIFIER | c.-3101G>A| |
S294 |
| 28602 | BAA01g20240 | A01 | 9944820 | G | A | missense_variant | MODERATE | c.55G>A|p.Glu19Lys |
S15 S3 |
| 28603 | BAA01g20240 | A01 | 9944948 | G | A | synonymous_variant | LOW | c.183G>A|p.Gln61Gln |
S13 |
| 28604 | BAA01g20260 | A01 | 9945482 | G | A | upstream_gene_variant | MODIFIER | c.-3480G>A| |
S95 |
| 28605 | BAA01g20240 | A01 | 9945500 | G | A | splice_region_variant&intron_variant | LOW | c.235-4G>A| |
S172 S217 |
| 28606 | BAA01g20250 | A01 | 9946111 | C | T | missense_variant | MODERATE | c.614G>A|p.Arg205Gln |
S48 |
| 28607 | BAA01g20250 | A01 | 9946304 | G | A | missense_variant | MODERATE | c.421C>T|p.Pro141Ser |
S229 |
| 28608 | BAA01g20250 | A01 | 9946420 | G | A | missense_variant | MODERATE | c.305C>T|p.Ser102Phe |
S94 |
| 28609 | BAA01g20250 | A01 | 9947018 | G | A | upstream_gene_variant | MODIFIER | c.-294C>T| |
S291 |
| 28610 | BAA01g20250 | A01 | 9947302 | C | T | upstream_gene_variant | MODIFIER | c.-578G>A| |
S104 S52 |
| 28611 | BAA01g20250 | A01 | 9948110 | G | A | upstream_gene_variant | MODIFIER | c.-1386C>T| |
S121 |
| 28612 | BAA01g20250 | A01 | 9948730 | G | A | upstream_gene_variant | MODIFIER | c.-2006C>T| |
S149 |
| 28613 | BAA01g20250 | A01 | 9949229 | C | T | upstream_gene_variant | MODIFIER | c.-2505G>A| |
S128 |
| 28614 | BAA01g20250 | A01 | 9949465 | G | A | upstream_gene_variant | MODIFIER | c.-2741C>T| |
S287 |
| 28615 | BAA01g20250 | A01 | 9949685 | C | T | upstream_gene_variant | MODIFIER | c.-2961G>A| |
S208 S93 |
| 28616 | BAA01g20260 | A01 | 9950321 | C | T | missense_variant | MODERATE | c.680C>T|p.Ser227Phe |
S151 S166 S167 S263 |
| 28617 | BAA01g20250 | A01 | 9950727 | G | A | upstream_gene_variant | MODIFIER | c.-4003C>T| |
S172 S217 |
| 28618 | BAA01g20250 | A01 | 9950857 | C | T | upstream_gene_variant | MODIFIER | c.-4133G>A| |
S146 |
| 28619 | BAA01g20250 | A01 | 9950886 | G | A | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S157 S163 |
| 28620 | BAA01g20250 | A01 | 9951073 | G | A | upstream_gene_variant | MODIFIER | c.-4349C>T| |
S292 |
| 28621 | BAA01g20270 | A01 | 9953167 | C | T | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S41 |
| 28622 | BAA01g20270 | A01 | 9953343 | C | T | synonymous_variant | LOW | c.675C>T|p.Leu225Leu |
S153 S273 |
| 28623 | BAA01g20270 | A01 | 9953421 | G | A | synonymous_variant | LOW | c.753G>A|p.Ser251Ser |
S162 |
| 28624 | BAA01g20290 | A01 | 9954163 | C | T | upstream_gene_variant | MODIFIER | c.-2870C>T| |
S230 |
| 28625 | BAA01g20290 | A01 | 9954441 | G | A | upstream_gene_variant | MODIFIER | c.-2592G>A| |
S298 |