Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19300 | A04 | 22821580 | G | A | downstream_gene_variant | MODIFIER | c.*4974C>T| |
S245 |
2 | BAA04g19300 | A04 | 22822138 | C | T | downstream_gene_variant | MODIFIER | c.*4416G>A| |
S246 |
3 | BAA04g19300 | A04 | 22822786 | G | A | downstream_gene_variant | MODIFIER | c.*3768C>T| |
S224 |
4 | BAA04g19300 | A04 | 22822877 | C | T | downstream_gene_variant | MODIFIER | c.*3677G>A| |
S43 |
5 | BAA04g19300 | A04 | 22823079 | G | A | downstream_gene_variant | MODIFIER | c.*3475C>T| |
S98 |
6 | BAA04g19300 | A04 | 22823127 | G | A | downstream_gene_variant | MODIFIER | c.*3427C>T| |
S203 |
7 | BAA04g19300 | A04 | 22823544 | C | T | downstream_gene_variant | MODIFIER | c.*3010G>A| |
S152 |
8 | BAA04g19300 | A04 | 22828809 | G | A | missense_variant | MODERATE | c.736C>T|p.Arg246Cys |
S239 |
9 | BAA04g19300 | A04 | 22828948 | G | A | synonymous_variant | LOW | c.681C>T|p.Val227Val |
S162 S39 |
10 | BAA04g19300 | A04 | 22829504 | C | T | missense_variant | MODERATE | c.488G>A|p.Ser163Asn |
S268 |
11 | BAA04g19300 | A04 | 22830529 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S38 |
12 | BAA04g19300 | A04 | 22831307 | C | T | upstream_gene_variant | MODIFIER | c.-886G>A| |
S172 S217 |
13 | BAA04g19300 | A04 | 22832216 | G | A | upstream_gene_variant | MODIFIER | c.-1795C>T| |
S201 |
14 | BAA04g19300 | A04 | 22833046 | C | T | upstream_gene_variant | MODIFIER | c.-2625G>A| |
S25 |
15 | BAA04g19300 | A04 | 22833048 | G | A | upstream_gene_variant | MODIFIER | c.-2627C>T| |
S273 |
16 | BAA04g19300 | A04 | 22833649 | C | T | upstream_gene_variant | MODIFIER | c.-3228G>A| |
S80 |
17 | BAA04g19300 | A04 | 22834525 | G | A | upstream_gene_variant | MODIFIER | c.-4104C>T| |
S206 S26 |
18 | BAA04g19300 | A04 | 22834771 | G | A | upstream_gene_variant | MODIFIER | c.-4350C>T| |
S12 S223 |
19 | BAA04g19300 | A04 | 22835147 | G | A | upstream_gene_variant | MODIFIER | c.-4726C>T| |
S269 |