| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145101 | BAA10g29750 | A10 | 22264844 | G | A | missense_variant | MODERATE | c.1490C>T|p.Pro497Leu |
S226 |
| 145102 | BAA10g29730 | A10 | 22266252 | C | T | downstream_gene_variant | MODIFIER | c.*4203C>T| |
S176 |
| 145103 | BAA10g29730 | A10 | 22266261 | G | A | downstream_gene_variant | MODIFIER | c.*4212G>A| |
S190 |
| 145104 | BAA10g29730 | A10 | 22266978 | C | T | downstream_gene_variant | MODIFIER | c.*4929C>T| |
S189 |
| 145105 | BAA10g29750 | A10 | 22267279 | G | A | synonymous_variant | LOW | c.273C>T|p.Ala91Ala |
S183 S198 |
| 145106 | BAA10g29750 | A10 | 22267335 | C | T | missense_variant | MODERATE | c.217G>A|p.Val73Ile |
S189 |
| 145107 | BAA10g29750 | A10 | 22268481 | C | T | upstream_gene_variant | MODIFIER | c.-930G>A| |
S277 |
| 145108 | BAA10g29750 | A10 | 22268564 | G | A | upstream_gene_variant | MODIFIER | c.-1013C>T| |
S167 |
| 145109 | BAA10g29750 | A10 | 22269458 | C | T | upstream_gene_variant | MODIFIER | c.-1907G>A| |
S162 |
| 145110 | BAA10g29750 | A10 | 22272049 | C | T | upstream_gene_variant | MODIFIER | c.-4498G>A| |
S234 |
| 145111 | BAA10g29760 | A10 | 22273143 | C | T | upstream_gene_variant | MODIFIER | c.-1120C>T| |
S229 |
| 145112 | BAA10g29760 | A10 | 22273164 | C | T | upstream_gene_variant | MODIFIER | c.-1099C>T| |
S14 |
| 145113 | BAA10g29760 | A10 | 22273217 | C | T | upstream_gene_variant | MODIFIER | c.-1046C>T| |
S73 S91 |
| 145114 | BAA10g29760 | A10 | 22273803 | G | A | upstream_gene_variant | MODIFIER | c.-460G>A| |
S298 |
| 145115 | BAA10g29760 | A10 | 22273804 | T | G | upstream_gene_variant | MODIFIER | c.-459T>G| |
S298 |
| 145116 | BAA10g29760 | A10 | 22274115 | G | A | upstream_gene_variant | MODIFIER | c.-148G>A| |
S106 |
| 145117 | BAA10g29760 | A10 | 22276638 | C | T | missense_variant | MODERATE | c.733C>T|p.Leu245Phe |
S211 |
| 145118 | BAA10g29770 | A10 | 22277860 | G | A | upstream_gene_variant | MODIFIER | c.-554G>A| |
S172 S217 |
| 145119 | BAA10g29770 | A10 | 22278783 | G | A | missense_variant | MODERATE | c.370G>A|p.Asp124Asn |
S35 |
| 145120 | BAA10g29780 | A10 | 22280385 | G | A | missense_variant | MODERATE | c.1211C>T|p.Pro404Leu |
S53 |
| 145121 | BAA10g29780 | A10 | 22280422 | C | T | missense_variant | MODERATE | c.1174G>A|p.Gly392Ser |
S242 |
| 145122 | BAA10g29760 | A10 | 22280458 | C | T | downstream_gene_variant | MODIFIER | c.*3001C>T| |
S246 |
| 145123 | BAA10g29760 | A10 | 22281775 | C | T | downstream_gene_variant | MODIFIER | c.*4318C>T| |
S296 |
| 145124 | BAA10g29790 | A10 | 22284817 | C | T | synonymous_variant | LOW | c.144G>A|p.Glu48Glu |
S56 |
| 145125 | BAA10g29780 | A10 | 22284997 | G | A | upstream_gene_variant | MODIFIER | c.-2569C>T| |
S284 |