Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g12370 | A08 | 10808371 | G | A | downstream_gene_variant | MODIFIER | c.*4763C>T| |
S212 S259 |
2 | BAA08g12370 | A08 | 10809153 | C | T | downstream_gene_variant | MODIFIER | c.*3981G>A| |
S235 |
3 | BAA08g12370 | A08 | 10810588 | G | A | downstream_gene_variant | MODIFIER | c.*2546C>T| |
S280 |
4 | BAA08g12370 | A08 | 10810987 | G | A | downstream_gene_variant | MODIFIER | c.*2147C>T| |
S35 |
5 | BAA08g12370 | A08 | 10811782 | G | A | downstream_gene_variant | MODIFIER | c.*1352C>T| |
S238 |
6 | BAA08g12370 | A08 | 10811907 | G | A | downstream_gene_variant | MODIFIER | c.*1227C>T| |
S298 |
7 | BAA08g12370 | A08 | 10811992 | C | T | downstream_gene_variant | MODIFIER | c.*1142G>A| |
S132 S137 S89 |
8 | BAA08g12370 | A08 | 10813785 | G | A | missense_variant | MODERATE | c.851C>T|p.Ser284Phe |
S211 |
9 | BAA08g12370 | A08 | 10813854 | G | A | missense_variant | MODERATE | c.782C>T|p.Ala261Val |
S257 |
10 | BAA08g12370 | A08 | 10814362 | C | T | missense_variant | MODERATE | c.274G>A|p.Val92Ile |
S134 |
11 | BAA08g12370 | A08 | 10814719 | C | T | intron_variant | MODIFIER | c.181-264G>A| |
S233 |
12 | BAA08g12370 | A08 | 10817190 | G | A | upstream_gene_variant | MODIFIER | c.-774C>T| |
S95 |
13 | BAA08g12370 | A08 | 10817400 | G | A | upstream_gene_variant | MODIFIER | c.-984C>T| |
S90 |
14 | BAA08g12370 | A08 | 10818223 | G | A | upstream_gene_variant | MODIFIER | c.-1807C>T| |
S172 S217 |
15 | BAA08g12370 | A08 | 10818277 | G | A | upstream_gene_variant | MODIFIER | c.-1861C>T| |
S174 |