Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19360 | A06 | 9996342 | G | A | downstream_gene_variant | MODIFIER | c.*3194C>T| |
S86 |
2 | BAA06g19360 | A06 | 9996559 | C | T | downstream_gene_variant | MODIFIER | c.*2977G>A| |
S236 |
3 | BAA06g19360 | A06 | 9996779 | C | T | downstream_gene_variant | MODIFIER | c.*2757G>A| |
S16 |
4 | BAA06g19360 | A06 | 9997082 | G | T | downstream_gene_variant | MODIFIER | c.*2454C>A| |
S159 S243 |
5 | BAA06g19360 | A06 | 9998771 | C | T | downstream_gene_variant | MODIFIER | c.*765G>A| |
S183 S198 |
6 | BAA06g19360 | A06 | 9999391 | C | T | downstream_gene_variant | MODIFIER | c.*145G>A| |
S155 |
7 | BAA06g19360 | A06 | 9999443 | C | T | downstream_gene_variant | MODIFIER | c.*93G>A| |
S178 |
8 | BAA06g19360 | A06 | 9999476 | C | T | downstream_gene_variant | MODIFIER | c.*60G>A| |
S98 |
9 | BAA06g19360 | A06 | 9999568 | C | T | missense_variant | MODERATE | c.1030G>A|p.Ala344Thr |
S259 |
10 | BAA06g19360 | A06 | 10002900 | C | T | intron_variant | MODIFIER | c.234+1273G>A| |
S200 |
11 | BAA06g19360 | A06 | 10003125 | C | T | intron_variant | MODIFIER | c.234+1048G>A| |
S6 |
12 | BAA06g19360 | A06 | 10004076 | G | A | intron_variant | MODIFIER | c.234+97C>T| |
S25 |
13 | BAA06g19360 | A06 | 10007738 | C | T | upstream_gene_variant | MODIFIER | c.-3332G>A| |
S155 S211 |
14 | BAA06g19360 | A06 | 10007784 | G | A | upstream_gene_variant | MODIFIER | c.-3378C>T| |
S161 |
15 | BAA06g19360 | A06 | 10008550 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S32 |
16 | BAA06g19360 | A06 | 10009302 | G | A | upstream_gene_variant | MODIFIER | c.-4896C>T| |
S59 |
17 | BAA06g19360 | A06 | 10009390 | G | A | upstream_gene_variant | MODIFIER | c.-4984C>T| |
S100 |