Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19350 | A10 | 17758320 | G | A | downstream_gene_variant | MODIFIER | c.*3199C>T| |
S59 |
2 | BAA10g19350 | A10 | 17758529 | G | A | downstream_gene_variant | MODIFIER | c.*2990C>T| |
S265 |
3 | BAA10g19350 | A10 | 17764574 | G | A | missense_variant | MODERATE | c.88C>T|p.Pro30Ser |
S62 |
4 | BAA10g19350 | A10 | 17765401 | C | T | upstream_gene_variant | MODIFIER | c.-740G>A| |
S266 |
5 | BAA10g19350 | A10 | 17766487 | G | A | upstream_gene_variant | MODIFIER | c.-1826C>T| |
S40 S49 |
6 | BAA10g19350 | A10 | 17767303 | T | A | upstream_gene_variant | MODIFIER | c.-2642A>T| |
S120 S121 S122 S174 S216 S23 S241 S265 S266 S27 S39 S55 S9 |
7 | BAA10g19350 | A10 | 17768197 | C | T | upstream_gene_variant | MODIFIER | c.-3536G>A| |
S11 |
8 | BAA10g19350 | A10 | 17769023 | C | T | upstream_gene_variant | MODIFIER | c.-4362G>A| |
S156 |
9 | BAA10g19350 | A10 | 17769328 | G | A | upstream_gene_variant | MODIFIER | c.-4667C>T| |
S38 |
10 | BAA10g19350 | A10 | 17769398 | G | A | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S291 |