| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 193901 | BAA02g27630 | A02 | 15552695 | G | A | upstream_gene_variant | MODIFIER | c.-3600G>A| |
S251 |
| 193902 | BAA02g27630 | A02 | 15553057 | C | T | upstream_gene_variant | MODIFIER | c.-3238C>T| |
S206 |
| 193903 | BAA02g27630 | A02 | 15553949 | C | T | upstream_gene_variant | MODIFIER | c.-2346C>T| |
S245 |
| 193904 | BAA02g27630 | A02 | 15555104 | G | A | upstream_gene_variant | MODIFIER | c.-1191G>A| |
S111 |
| 193905 | BAA02g27630 | A02 | 15555798 | C | T | upstream_gene_variant | MODIFIER | c.-497C>T| |
S160 |
| 193906 | BAA02g27630 | A02 | 15556711 | G | A | missense_variant | MODERATE | c.341G>A|p.Gly114Glu |
S150 |
| 193907 | BAA02g27630 | A02 | 15557184 | C | T | missense_variant | MODERATE | c.641C>T|p.Ala214Val |
S262 |
| 193908 | BAA02g27630 | A02 | 15558424 | C | T | downstream_gene_variant | MODIFIER | c.*579C>T| |
S296 |
| 193909 | BAA02g27630 | A02 | 15559039 | G | A | downstream_gene_variant | MODIFIER | c.*1194G>A| |
S272 |
| 193910 | BAA02g27630 | A02 | 15560473 | C | T | downstream_gene_variant | MODIFIER | c.*2628C>T| |
S216 |
| 193911 | BAA02g27640 | A02 | 15561794 | C | T | synonymous_variant | LOW | c.108G>A|p.Arg36Arg |
S203 |
| 193912 | BAA02g27640 | A02 | 15562698 | C | T | upstream_gene_variant | MODIFIER | c.-797G>A| |
S42 |
| 193913 | BAA02g27640 | A02 | 15563125 | G | A | upstream_gene_variant | MODIFIER | c.-1224C>T| |
S293 |
| 193914 | BAA02g27640 | A02 | 15563487 | G | A | upstream_gene_variant | MODIFIER | c.-1586C>T| |
S136 |
| 193915 | BAA02g27640 | A02 | 15566425 | G | A | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S60 |
| 193916 | BAA02g27660 | A02 | 15568002 | G | A | upstream_gene_variant | MODIFIER | c.-873G>A| |
S19 |
| 193917 | BAA02g27660 | A02 | 15568849 | C | T | upstream_gene_variant | MODIFIER | c.-26C>T| |
S115 |
| 193918 | BAA02g27660 | A02 | 15568966 | G | A | missense_variant | MODERATE | c.92G>A|p.Gly31Asp |
S293 |
| 193919 | BAA02g27660 | A02 | 15569061 | G | A | missense_variant | MODERATE | c.187G>A|p.Asp63Asn |
S202 |
| 193920 | BAA02g27660 | A02 | 15569393 | G | A | synonymous_variant | LOW | c.519G>A|p.Gln173Gln |
S202 |
| 193921 | BAA02g27660 | A02 | 15569473 | C | T | missense_variant | MODERATE | c.599C>T|p.Pro200Leu |
S268 |
| 193922 | BAA02g27660 | A02 | 15569530 | G | A | missense_variant | MODERATE | c.656G>A|p.Ser219Asn |
S251 |
| 193923 | BAA02g27660 | A02 | 15573372 | C | T | downstream_gene_variant | MODIFIER | c.*3814C>T| |
S167 |
| 193924 | BAA02g27660 | A02 | 15574326 | G | A | downstream_gene_variant | MODIFIER | c.*4768G>A| |
S37 |
| 193925 | BAA02g27660-BAA02g27670 | A02 | 15575010 | G | A | intergenic_region | MODIFIER | n.15575010G>A| |
S159 S243 |