Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18610 | A08 | 14847767 | C | T | upstream_gene_variant | MODIFIER | c.-4340C>T| |
S284 |
2 | BAA08g18610 | A08 | 14849357 | C | T | upstream_gene_variant | MODIFIER | c.-2750C>T| |
S104 S52 |
3 | BAA08g18610 | A08 | 14849808 | C | T | upstream_gene_variant | MODIFIER | c.-2299C>T| |
S184 |
4 | BAA08g18610 | A08 | 14849825 | T | G | upstream_gene_variant | MODIFIER | c.-2282T>G| |
S10 S147 S157 S233 S243 S301 S74 |
5 | BAA08g18610 | A08 | 14850115 | G | A | upstream_gene_variant | MODIFIER | c.-1992G>A| |
S48 |
6 | BAA08g18610 | A08 | 14850409 | C | T | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S2 |
7 | BAA08g18610 | A08 | 14852172 | G | A | synonymous_variant | LOW | c.66G>A|p.Lys22Lys |
S32 |
8 | BAA08g18610 | A08 | 14852315 | G | A | missense_variant&splice_region_variant | MODERATE | c.97G>A|p.Val33Ile |
S13 |
9 | BAA08g18610 | A08 | 14852451 | G | A | missense_variant | MODERATE | c.233G>A|p.Gly78Glu |
S257 |
10 | BAA08g18610 | A08 | 14853230 | G | A | missense_variant | MODERATE | c.586G>A|p.Ala196Thr |
S164 |
11 | BAA08g18610 | A08 | 14853314 | C | T | missense_variant | MODERATE | c.670C>T|p.Pro224Ser |
S168 |
12 | BAA08g18610 | A08 | 14853538 | G | A | missense_variant | MODERATE | c.800G>A|p.Gly267Asp |
S61 |