| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 85101 | BAA01g45090 | A01 | 30060935 | G | A | missense_variant | MODERATE | c.49G>A|p.Glu17Lys |
S236 |
| 85102 | BAA01g45090 | A01 | 30061019 | C | T | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S58 |
| 85103 | BAA01g45100 | A01 | 30061946 | C | T | upstream_gene_variant | MODIFIER | c.-2434C>T| |
S65 |
| 85104 | BAA01g45090 | A01 | 30062854 | C | T | missense_variant | MODERATE | c.1250C>T|p.Ser417Leu |
S7 |
| 85105 | BAA01g45100 | A01 | 30063207 | G | A | upstream_gene_variant | MODIFIER | c.-1173G>A| |
S268 |
| 85106 | BAA01g45100 | A01 | 30064280 | C | T | upstream_gene_variant | MODIFIER | c.-100C>T| |
S156 |
| 85107 | BAA01g45110 | A01 | 30064821 | G | A | upstream_gene_variant | MODIFIER | c.-1610G>A| |
S197 |
| 85108 | BAA01g45100 | A01 | 30064973 | G | A | missense_variant | MODERATE | c.505G>A|p.Asp169Asn |
S61 |
| 85109 | BAA01g45110 | A01 | 30065373 | C | T | upstream_gene_variant | MODIFIER | c.-1058C>T| |
S120 |
| 85110 | BAA01g45110 | A01 | 30066633 | T | G | missense_variant | MODERATE | c.203T>G|p.Val68Gly |
S163 S165 S235 S236 S66 |
| 85111 | BAA01g45110 | A01 | 30067325 | G | A | missense_variant | MODERATE | c.895G>A|p.Asp299Asn |
S151 |
| 85112 | BAA01g45110 | A01 | 30067357 | C | T | synonymous_variant | LOW | c.927C>T|p.Thr309Thr |
S58 |
| 85113 | BAA01g45120 | A01 | 30068025 | C | T | missense_variant | MODERATE | c.1889G>A|p.Cys630Tyr |
S130 |
| 85114 | BAA01g45120 | A01 | 30068081 | C | T | synonymous_variant | LOW | c.1833G>A|p.Lys611Lys |
S239 |
| 85115 | BAA01g45120 | A01 | 30068297 | C | T | missense_variant&splice_region_variant | MODERATE | c.1700G>A|p.Arg567Lys |
S216 |
| 85116 | BAA01g45120 | A01 | 30068618 | C | T | missense_variant | MODERATE | c.1379G>A|p.Arg460Lys |
S237 |
| 85117 | BAA01g45130 | A01 | 30069122 | G | A | upstream_gene_variant | MODIFIER | c.-2718G>A| |
S87 |
| 85118 | BAA01g45120 | A01 | 30069384 | C | T | missense_variant | MODERATE | c.945G>A|p.Met315Ile |
S88 |
| 85119 | BAA01g45120 | A01 | 30069516 | G | A | synonymous_variant | LOW | c.813C>T|p.Phe271Phe |
S158 |
| 85120 | BAA01g45120 | A01 | 30069783 | C | T | synonymous_variant | LOW | c.546G>A|p.Ala182Ala |
S263 |
| 85121 | BAA01g45120 | A01 | 30069905 | C | T | missense_variant | MODERATE | c.508G>A|p.Asp170Asn |
S132 S215 |
| 85122 | BAA01g45120 | A01 | 30070159 | G | A | missense_variant | MODERATE | c.343C>T|p.Pro115Ser |
S122 |
| 85123 | BAA01g45130 | A01 | 30072387 | C | T | synonymous_variant | LOW | c.243C>T|p.Leu81Leu |
S38 |
| 85124 | BAA01g45120 | A01 | 30072563 | C | T | upstream_gene_variant | MODIFIER | c.-1928G>A| |
S165 |
| 85125 | BAA01g45140 | A01 | 30073993 | C | T | missense_variant | MODERATE | c.1394G>A|p.Gly465Glu |
S260 |