| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 49701 | BAA01g28150 | A01 | 17206981 | C | T | upstream_gene_variant | MODIFIER | c.-3247G>A| |
S198 |
| 49702 | BAA01g28150 | A01 | 17207663 | G | A | upstream_gene_variant | MODIFIER | c.-3929C>T| |
S299 |
| 49703 | BAA01g28160 | A01 | 17210731 | G | A | upstream_gene_variant | MODIFIER | c.-2687G>A| |
S283 |
| 49704 | BAA01g28160 | A01 | 17212139 | C | T | upstream_gene_variant | MODIFIER | c.-1279C>T| |
S162 |
| 49705 | BAA01g28160 | A01 | 17213434 | C | T | missense_variant | MODERATE | c.17C>T|p.Pro6Leu |
S11 |
| 49706 | BAA01g28160 | A01 | 17213526 | C | T | missense_variant | MODERATE | c.109C>T|p.Pro37Ser |
S196 |
| 49707 | BAA01g28160 | A01 | 17213949 | G | A | missense_variant | MODERATE | c.532G>A|p.Ala178Thr |
S7 |
| 49708 | BAA01g28160 | A01 | 17214066 | G | A | missense_variant | MODERATE | c.649G>A|p.Asp217Asn |
S25 |
| 49709 | BAA01g28160 | A01 | 17214608 | C | T | synonymous_variant | LOW | c.1101C>T|p.Asn367Asn |
S240 |
| 49710 | BAA01g28170 | A01 | 17214680 | C | T | downstream_gene_variant | MODIFIER | c.*2853G>A| |
S249 |
| 49711 | BAA01g28160 | A01 | 17216575 | G | A | downstream_gene_variant | MODIFIER | c.*1496G>A| |
S150 |
| 49712 | BAA01g28160 | A01 | 17217059 | C | T | downstream_gene_variant | MODIFIER | c.*1980C>T| |
S75 S81 |
| 49713 | BAA01g28160 | A01 | 17217370 | G | A | downstream_gene_variant | MODIFIER | c.*2291G>A| |
S216 |
| 49714 | BAA01g28170 | A01 | 17218072 | G | A | missense_variant | MODERATE | c.980C>T|p.Ser327Phe |
S292 |
| 49715 | BAA01g28170 | A01 | 17218755 | C | T | missense_variant | MODERATE | c.742G>A|p.Asp248Asn |
S53 |
| 49716 | BAA01g28170 | A01 | 17219761 | G | A | missense_variant | MODERATE | c.62C>T|p.Ser21Phe |
S15 S3 |
| 49717 | BAA01g28170 | A01 | 17220101 | C | T | upstream_gene_variant | MODIFIER | c.-279G>A| |
S44 |
| 49718 | BAA01g28170 | A01 | 17220135 | G | A | upstream_gene_variant | MODIFIER | c.-313C>T| |
S23 |
| 49719 | BAA01g28170 | A01 | 17220322 | C | T | upstream_gene_variant | MODIFIER | c.-500G>A| |
S192 |
| 49720 | BAA01g28170 | A01 | 17221218 | G | A | upstream_gene_variant | MODIFIER | c.-1396C>T| |
S292 |
| 49721 | BAA01g28180 | A01 | 17222049 | G | A | missense_variant | MODERATE | c.431C>T|p.Ser144Leu |
S172 S217 |
| 49722 | BAA01g28170 | A01 | 17223072 | G | A | upstream_gene_variant | MODIFIER | c.-3250C>T| |
S271 |
| 49723 | BAA01g28170 | A01 | 17224778 | C | T | upstream_gene_variant | MODIFIER | c.-4956G>A| |
S183 |
| 49724 | BAA01g28180 | A01 | 17225120 | G | A | upstream_gene_variant | MODIFIER | c.-2260C>T| |
S244 |
| 49725 | BAA01g28180 | A01 | 17225500 | C | T | upstream_gene_variant | MODIFIER | c.-2640G>A| |
S293 |