Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21250 | A01 | 10534433 | C | T | upstream_gene_variant | MODIFIER | c.-4726C>T| |
S182 |
2 | BAA01g21250 | A01 | 10534745 | G | A | upstream_gene_variant | MODIFIER | c.-4414G>A| |
S144 |
3 | BAA01g21250 | A01 | 10534972 | C | T | upstream_gene_variant | MODIFIER | c.-4187C>T| |
S68 |
4 | BAA01g21250 | A01 | 10535050 | C | T | upstream_gene_variant | MODIFIER | c.-4109C>T| |
S208 S219 |
5 | BAA01g21250 | A01 | 10535515 | G | A | upstream_gene_variant | MODIFIER | c.-3644G>A| |
S204 |
6 | BAA01g21250 | A01 | 10535524 | G | A | upstream_gene_variant | MODIFIER | c.-3635G>A| |
S280 |
7 | BAA01g21250 | A01 | 10536316 | G | A | upstream_gene_variant | MODIFIER | c.-2843G>A| |
S298 |
8 | BAA01g21250 | A01 | 10537771 | C | T | upstream_gene_variant | MODIFIER | c.-1388C>T| |
S140 |
9 | BAA01g21250 | A01 | 10538166 | C | T | upstream_gene_variant | MODIFIER | c.-993C>T| |
S266 |
10 | BAA01g21250 | A01 | 10538272 | C | T | upstream_gene_variant | MODIFIER | c.-887C>T| |
S266 |
11 | BAA01g21250 | A01 | 10538287 | G | A | upstream_gene_variant | MODIFIER | c.-872G>A| |
S249 |
12 | BAA01g21250 | A01 | 10538297 | C | T | upstream_gene_variant | MODIFIER | c.-862C>T| |
S1 S90 |
13 | BAA01g21250 | A01 | 10538413 | C | T | upstream_gene_variant | MODIFIER | c.-746C>T| |
S81 S85 |
14 | BAA01g21250 | A01 | 10538626 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S146 |
15 | BAA01g21250 | A01 | 10538752 | C | T | upstream_gene_variant | MODIFIER | c.-407C>T| |
S18 |
16 | BAA01g21250 | A01 | 10540044 | G | A | splice_donor_variant&intron_variant | HIGH | c.369+1G>A| |
S280 |
17 | BAA01g21250 | A01 | 10540246 | G | A | missense_variant | MODERATE | c.485G>A|p.Arg162Lys |
S124 |
18 | BAA01g21250 | A01 | 10540361 | C | T | synonymous_variant | LOW | c.600C>T|p.Leu200Leu |
S78 |