| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 191901 | BAA02g26620 | A02 | 14898001 | C | T | downstream_gene_variant | MODIFIER | c.*25G>A| |
S176 |
| 191902 | BAA02g26620 | A02 | 14899006 | G | A | upstream_gene_variant | MODIFIER | c.-183C>T| |
S133 |
| 191903 | BAA02g26630 | A02 | 14901671 | C | T | missense_variant | MODERATE | c.406G>A|p.Glu136Lys |
S250 |
| 191904 | BAA02g26630 | A02 | 14902147 | C | T | missense_variant | MODERATE | c.230G>A|p.Gly77Asp |
S157 S163 |
| 191905 | BAA02g26620 | A02 | 14903483 | G | A | upstream_gene_variant | MODIFIER | c.-4660C>T| |
S128 |
| 191906 | BAA02g26620 | A02 | 14903576 | G | A | upstream_gene_variant | MODIFIER | c.-4753C>T| |
S10 |
| 191907 | BAA02g26620 | A02 | 14903765 | C | T | upstream_gene_variant | MODIFIER | c.-4942G>A| |
S283 |
| 191908 | BAA02g26630 | A02 | 14903975 | G | A | upstream_gene_variant | MODIFIER | c.-1599C>T| |
S236 S262 S263 |
| 191909 | BAA02g26630 | A02 | 14904194 | G | A | upstream_gene_variant | MODIFIER | c.-1818C>T| |
S126 |
| 191910 | BAA02g26630 | A02 | 14905096 | A | G | upstream_gene_variant | MODIFIER | c.-2720T>C| |
S250 |
| 191911 | BAA02g26640 | A02 | 14905900 | G | A | missense_variant | MODERATE | c.644G>A|p.Arg215His |
S94 |
| 191912 | BAA02g26630 | A02 | 14906603 | G | A | upstream_gene_variant | MODIFIER | c.-4227C>T| |
S57 |
| 191913 | BAA02g26630 | A02 | 14906803 | G | A | upstream_gene_variant | MODIFIER | c.-4427C>T| |
S291 |
| 191914 | BAA02g26650 | A02 | 14907983 | G | A | upstream_gene_variant | MODIFIER | c.-679G>A| |
S288 |
| 191915 | BAA02g26650 | A02 | 14908276 | C | T | upstream_gene_variant | MODIFIER | c.-386C>T| |
S40 S49 |
| 191916 | BAA02g26650 | A02 | 14909070 | G | A | missense_variant | MODERATE | c.409G>A|p.Glu137Lys |
S291 |
| 191917 | BAA02g26650 | A02 | 14909075 | G | A | missense_variant | MODERATE | c.414G>A|p.Met138Ile |
S159 S243 |
| 191918 | BAA02g26640 | A02 | 14909217 | G | A | downstream_gene_variant | MODIFIER | c.*3097G>A| |
S291 |
| 191919 | BAA02g26640 | A02 | 14909442 | C | T | downstream_gene_variant | MODIFIER | c.*3322C>T| |
S277 |
| 191920 | BAA02g26640 | A02 | 14910489 | G | A | downstream_gene_variant | MODIFIER | c.*4369G>A| |
S187 |
| 191921 | BAA02g26650 | A02 | 14912106 | G | A | downstream_gene_variant | MODIFIER | c.*1092G>A| |
S13 |
| 191922 | BAA02g26650 | A02 | 14912346 | C | T | downstream_gene_variant | MODIFIER | c.*1332C>T| |
S266 |
| 191923 | BAA02g26650 | A02 | 14912486 | G | A | downstream_gene_variant | MODIFIER | c.*1472G>A| |
S68 |
| 191924 | BAA02g26660 | A02 | 14914222 | C | T | upstream_gene_variant | MODIFIER | c.-4307C>T| |
S81 |
| 191925 | BAA02g26660 | A02 | 14914495 | C | T | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S11 |