Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g27450 | A05 | 31715871 | C | T | downstream_gene_variant | MODIFIER | c.*3435G>A| |
S105 S106 |
2 | BAA05g27450 | A05 | 31715982 | G | A | downstream_gene_variant | MODIFIER | c.*3324C>T| |
S172 |
3 | BAA05g27450 | A05 | 31716045 | G | A | downstream_gene_variant | MODIFIER | c.*3261C>T| |
S97 |
4 | BAA05g27450 | A05 | 31717023 | G | A | downstream_gene_variant | MODIFIER | c.*2283C>T| |
S78 |
5 | BAA05g27450 | A05 | 31717566 | C | T | downstream_gene_variant | MODIFIER | c.*1740G>A| |
S162 |
6 | BAA05g27450 | A05 | 31717875 | G | A | downstream_gene_variant | MODIFIER | c.*1431C>T| |
S13 |
7 | BAA05g27450 | A05 | 31718217 | C | T | downstream_gene_variant | MODIFIER | c.*1089G>A| |
S113 |
8 | BAA05g27450 | A05 | 31718857 | G | A | downstream_gene_variant | MODIFIER | c.*449C>T| |
S156 S20 |
9 | BAA05g27450 | A05 | 31719892 | G | A | missense_variant | MODERATE | c.860C>T|p.Thr287Ile |
S39 |
10 | BAA05g27450 | A05 | 31721040 | C | T | intron_variant | MODIFIER | c.12-218G>A| |
S237 |
11 | BAA05g27450 | A05 | 31721529 | G | A | upstream_gene_variant | MODIFIER | c.-70C>T| |
S85 |
12 | BAA05g27450 | A05 | 31721886 | G | A | upstream_gene_variant | MODIFIER | c.-427C>T| |
S77 S82 |
13 | BAA05g27450 | A05 | 31722069 | G | A | upstream_gene_variant | MODIFIER | c.-610C>T| |
S308 |
14 | BAA05g27450 | A05 | 31722584 | G | A | upstream_gene_variant | MODIFIER | c.-1125C>T| |
S174 S216 S241 S27 S39 |
15 | BAA05g27450 | A05 | 31722719 | G | A | upstream_gene_variant | MODIFIER | c.-1260C>T| |
S11 |
16 | BAA05g27450 | A05 | 31723376 | G | A | upstream_gene_variant | MODIFIER | c.-1917C>T| |
S186 |
17 | BAA05g27450 | A05 | 31723598 | G | A | upstream_gene_variant | MODIFIER | c.-2139C>T| |
S20 |
18 | BAA05g27450 | A05 | 31724979 | G | A | upstream_gene_variant | MODIFIER | c.-3520C>T| |
S221 |
19 | BAA05g27450 | A05 | 31726423 | C | T | upstream_gene_variant | MODIFIER | c.-4964G>A| |
S89 |