Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14770 | A10 | 15405208 | G | A | upstream_gene_variant | MODIFIER | c.-4778G>A| |
S13 |
2 | BAA10g14770 | A10 | 15405254 | C | T | upstream_gene_variant | MODIFIER | c.-4732C>T| |
S183 |
3 | BAA10g14770 | A10 | 15405840 | C | T | upstream_gene_variant | MODIFIER | c.-4146C>T| |
S284 |
4 | BAA10g14770 | A10 | 15406274 | C | T | upstream_gene_variant | MODIFIER | c.-3712C>T| |
S275 |
5 | BAA10g14770 | A10 | 15407585 | C | T | upstream_gene_variant | MODIFIER | c.-2401C>T| |
S133 |
6 | BAA10g14770 | A10 | 15410195 | C | T | synonymous_variant | LOW | c.210C>T|p.His70His |
S247 |
7 | BAA10g14770 | A10 | 15410659 | G | A | missense_variant | MODERATE | c.674G>A|p.Gly225Glu |
S174 S216 S241 S265 S39 |
8 | BAA10g14770 | A10 | 15410760 | G | A | missense_variant | MODERATE | c.775G>A|p.Glu259Lys |
S198 |
9 | BAA10g14770 | A10 | 15413131 | C | T | downstream_gene_variant | MODIFIER | c.*2018C>T| |
S84 S93 |
10 | BAA10g14770 | A10 | 15413145 | G | A | downstream_gene_variant | MODIFIER | c.*2032G>A| |
S169 |
11 | BAA10g14770 | A10 | 15413312 | C | T | downstream_gene_variant | MODIFIER | c.*2199C>T| |
S156 |
12 | BAA10g14770 | A10 | 15415031 | G | A | downstream_gene_variant | MODIFIER | c.*3918G>A| |
S18 |