| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 27201 | BAA01g19270 | A01 | 9483121 | G | A | missense_variant | MODERATE | c.1597G>A|p.Glu533Lys |
S262 |
| 27202 | BAA01g19270 | A01 | 9483229 | C | T | missense_variant | MODERATE | c.1705C>T|p.Leu569Phe |
S84 |
| 27203 | BAA01g19270 | A01 | 9483284 | C | T | missense_variant | MODERATE | c.1760C>T|p.Thr587Ile |
S287 |
| 27204 | BAA01g19280 | A01 | 9483529 | G | A | missense_variant | MODERATE | c.1823C>T|p.Ser608Phe |
S94 |
| 27205 | BAA01g19280 | A01 | 9483652 | G | A | missense_variant | MODERATE | c.1700C>T|p.Ala567Val |
S105 S106 |
| 27206 | BAA01g19260 | A01 | 9484495 | G | A | upstream_gene_variant | MODIFIER | c.-4636C>T| |
S103 |
| 27207 | BAA01g19260 | A01 | 9484753 | G | A | upstream_gene_variant | MODIFIER | c.-4894C>T| |
S224 |
| 27208 | BAA01g19270 | A01 | 9485048 | C | T | downstream_gene_variant | MODIFIER | c.*1697C>T| |
S168 |
| 27209 | BAA01g19280 | A01 | 9485136 | C | T | missense_variant | MODERATE | c.1498G>A|p.Asp500Asn |
S113 |
| 27210 | BAA01g19280 | A01 | 9485889 | C | T | missense_variant | MODERATE | c.868G>A|p.Glu290Lys |
S270 |
| 27211 | BAA01g19280 | A01 | 9486923 | G | A | upstream_gene_variant | MODIFIER | c.-167C>T| |
S157 |
| 27212 | BAA01g19280 | A01 | 9487079 | G | A | upstream_gene_variant | MODIFIER | c.-323C>T| |
S13 |
| 27213 | BAA01g19280 | A01 | 9487930 | C | T | upstream_gene_variant | MODIFIER | c.-1174G>A| |
S4 |
| 27214 | BAA01g19280 | A01 | 9488585 | C | T | upstream_gene_variant | MODIFIER | c.-1829G>A| |
S100 |
| 27215 | BAA01g19280 | A01 | 9489213 | C | T | upstream_gene_variant | MODIFIER | c.-2457G>A| |
S303 |
| 27216 | BAA01g19280 | A01 | 9489789 | C | T | upstream_gene_variant | MODIFIER | c.-3033G>A| |
S128 |
| 27217 | BAA01g19290 | A01 | 9491226 | G | A | missense_variant | MODERATE | c.677G>A|p.Arg226Gln |
S72 S78 |
| 27218 | BAA01g19290 | A01 | 9491555 | G | T | missense_variant | MODERATE | c.1006G>T|p.Gly336Cys |
S144 |
| 27219 | BAA01g19290 | A01 | 9492409 | C | T | missense_variant | MODERATE | c.1801C>T|p.Pro601Ser |
S44 |
| 27220 | BAA01g19290 | A01 | 9492812 | G | A | missense_variant | MODERATE | c.2204G>A|p.Arg735His |
S127 |
| 27221 | BAA01g19300 | A01 | 9493759 | G | A | upstream_gene_variant | MODIFIER | c.-2836G>A| |
S195 |
| 27222 | BAA01g19300 | A01 | 9494210 | G | A | upstream_gene_variant | MODIFIER | c.-2385G>A| |
S245 |
| 27223 | BAA01g19300 | A01 | 9494293 | G | A | upstream_gene_variant | MODIFIER | c.-2302G>A| |
S175 |
| 27224 | BAA01g19300 | A01 | 9494530 | G | A | upstream_gene_variant | MODIFIER | c.-2065G>A| |
S84 S93 |
| 27225 | BAA01g19300 | A01 | 9494565 | C | T | upstream_gene_variant | MODIFIER | c.-2030C>T| |
S39 |