| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 177151 | BAA02g18690 | A02 | 9592367 | G | A | intron_variant | MODIFIER | c.6826-36C>T| |
S43 |
| 177152 | BAA02g18690 | A02 | 9592410 | G | A | missense_variant&splice_region_variant | MODERATE | c.6824C>T|p.Thr2275Met |
S17 |
| 177153 | BAA02g18690 | A02 | 9592764 | G | A | missense_variant | MODERATE | c.6470C>T|p.Ser2157Phe |
S125 |
| 177154 | BAA02g18690 | A02 | 9592812 | G | A | missense_variant | MODERATE | c.6422C>T|p.Ala2141Val |
S150 |
| 177155 | BAA02g18690 | A02 | 9593057 | C | T | synonymous_variant | LOW | c.6177G>A|p.Glu2059Glu |
S216 |
| 177156 | BAA02g18690 | A02 | 9593935 | G | A | missense_variant | MODERATE | c.5387C>T|p.Ser1796Phe |
S86 S98 |
| 177157 | BAA02g18690 | A02 | 9594588 | G | A | synonymous_variant | LOW | c.4734C>T|p.Asn1578Asn |
S5 |
| 177158 | BAA02g18690 | A02 | 9595741 | G | A | intron_variant | MODIFIER | c.3957+58C>T| |
S189 |
| 177159 | BAA02g18690 | A02 | 9596506 | C | T | missense_variant | MODERATE | c.3250G>A|p.Ala1084Thr |
S195 |
| 177160 | BAA02g18690 | A02 | 9596512 | G | A | missense_variant | MODERATE | c.3244C>T|p.Leu1082Phe |
S168 |
| 177161 | BAA02g18690 | A02 | 9597256 | G | A | synonymous_variant | LOW | c.2500C>T|p.Leu834Leu |
S272 |
| 177162 | BAA02g18690 | A02 | 9597398 | C | T | synonymous_variant | LOW | c.2358G>A|p.Lys786Lys |
S18 |
| 177163 | BAA02g18700 | A02 | 9597782 | G | A | downstream_gene_variant | MODIFIER | c.*4169C>T| |
S11 |
| 177164 | BAA02g18700 | A02 | 9600796 | G | A | downstream_gene_variant | MODIFIER | c.*1155C>T| |
S126 |
| 177165 | BAA02g18690 | A02 | 9601622 | G | A | upstream_gene_variant | MODIFIER | c.-51C>T| |
S128 |
| 177166 | BAA02g18690 | A02 | 9601694 | G | A | upstream_gene_variant | MODIFIER | c.-123C>T| |
S223 |
| 177167 | BAA02g18700 | A02 | 9602057 | G | A | missense_variant | MODERATE | c.812C>T|p.Ser271Phe |
S59 |
| 177168 | BAA02g18690 | A02 | 9602475 | C | T | upstream_gene_variant | MODIFIER | c.-904G>A| |
S181 |
| 177169 | BAA02g18690 | A02 | 9603148 | C | T | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S183 S198 |
| 177170 | BAA02g18690 | A02 | 9604114 | C | T | upstream_gene_variant | MODIFIER | c.-2543G>A| |
S119 |
| 177171 | BAA02g18690 | A02 | 9604120 | C | T | upstream_gene_variant | MODIFIER | c.-2549G>A| |
S189 |
| 177172 | BAA02g18690 | A02 | 9604177 | G | A | upstream_gene_variant | MODIFIER | c.-2606C>T| |
S45 |
| 177173 | BAA02g18690 | A02 | 9605213 | G | A | upstream_gene_variant | MODIFIER | c.-3642C>T| |
S168 |
| 177174 | BAA02g18690 | A02 | 9605296 | G | A | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S283 |
| 177175 | BAA02g18690 | A02 | 9605410 | C | T | upstream_gene_variant | MODIFIER | c.-3839G>A| |
S124 |