Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g27970 | A05 | 32029524 | G | A | downstream_gene_variant | MODIFIER | c.*4133C>T| |
S234 |
2 | BAA05g27970 | A05 | 32030047 | G | A | downstream_gene_variant | MODIFIER | c.*3610C>T| |
S14 |
3 | BAA05g27970 | A05 | 32031465 | C | T | downstream_gene_variant | MODIFIER | c.*2192G>A| |
S174 S175 |
4 | BAA05g27970 | A05 | 32031525 | C | T | downstream_gene_variant | MODIFIER | c.*2132G>A| |
S164 |
5 | BAA05g27970 | A05 | 32032124 | C | T | downstream_gene_variant | MODIFIER | c.*1533G>A| |
S157 |
6 | BAA05g27970 | A05 | 32032489 | G | A | downstream_gene_variant | MODIFIER | c.*1168C>T| |
S197 |
7 | BAA05g27970 | A05 | 32032881 | G | A | downstream_gene_variant | MODIFIER | c.*776C>T| |
S257 |
8 | BAA05g27970 | A05 | 32034193 | G | A | intron_variant | MODIFIER | c.325-9C>T| |
S80 |
9 | BAA05g27970 | A05 | 32034734 | G | A | missense_variant | MODERATE | c.244C>T|p.Pro82Ser |
S306 |
10 | BAA05g27970 | A05 | 32035171 | C | T | upstream_gene_variant | MODIFIER | c.-194G>A| |
S18 |
11 | BAA05g27970 | A05 | 32037456 | C | T | upstream_gene_variant | MODIFIER | c.-2479G>A| |
S183 S198 |
12 | BAA05g27970 | A05 | 32037506 | C | T | upstream_gene_variant | MODIFIER | c.-2529G>A| |
S92 |
13 | BAA05g27970 | A05 | 32037521 | C | T | upstream_gene_variant | MODIFIER | c.-2544G>A| |
S204 |
14 | BAA05g27970 | A05 | 32037695 | C | T | upstream_gene_variant | MODIFIER | c.-2718G>A| |
S81 |
15 | BAA05g27970 | A05 | 32037752 | C | T | upstream_gene_variant | MODIFIER | c.-2775G>A| |
S153 S213 |
16 | BAA05g27970 | A05 | 32037913 | G | A | upstream_gene_variant | MODIFIER | c.-2936C>T| |
S11 |
17 | BAA05g27970 | A05 | 32039073 | G | A | upstream_gene_variant | MODIFIER | c.-4096C>T| |
S238 |
18 | BAA05g27970 | A05 | 32039569 | C | T | upstream_gene_variant | MODIFIER | c.-4592G>A| |
S261 |
19 | BAA05g27970 | A05 | 32039763 | C | T | upstream_gene_variant | MODIFIER | c.-4786G>A| |
S292 |