Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08090 | A04 | 5497546 | C | T | upstream_gene_variant | MODIFIER | c.-4558C>T| |
S110 S240 |
2 | BAA04g08090 | A04 | 5497897 | C | T | upstream_gene_variant | MODIFIER | c.-4207C>T| |
S140 |
3 | BAA04g08090 | A04 | 5497950 | C | T | upstream_gene_variant | MODIFIER | c.-4154C>T| |
S168 |
4 | BAA04g08090 | A04 | 5497987 | G | A | upstream_gene_variant | MODIFIER | c.-4117G>A| |
S238 |
5 | BAA04g08090 | A04 | 5497996 | G | A | upstream_gene_variant | MODIFIER | c.-4108G>A| |
S193 |
6 | BAA04g08090 | A04 | 5498432 | C | T | upstream_gene_variant | MODIFIER | c.-3672C>T| |
S260 |
7 | BAA04g08090 | A04 | 5498726 | C | T | upstream_gene_variant | MODIFIER | c.-3378C>T| |
S289 S290 |
8 | BAA04g08090 | A04 | 5499094 | G | A | upstream_gene_variant | MODIFIER | c.-3010G>A| |
S275 |
9 | BAA04g08090 | A04 | 5499266 | C | T | upstream_gene_variant | MODIFIER | c.-2838C>T| |
S301 S304 |
10 | BAA04g08090 | A04 | 5501300 | G | A | upstream_gene_variant | MODIFIER | c.-804G>A| |
S160 |
11 | BAA04g08090 | A04 | 5502262 | C | T | missense_variant | MODERATE | c.76C>T|p.His26Tyr |
S30 S31 |
12 | BAA04g08090 | A04 | 5502641 | C | T | missense_variant | MODERATE | c.455C>T|p.Pro152Leu |
S239 |
13 | BAA04g08090 | A04 | 5503284 | G | A | synonymous_variant | LOW | c.1098G>A|p.Thr366Thr |
S262 |
14 | BAA04g08090 | A04 | 5503477 | G | A | missense_variant | MODERATE | c.1291G>A|p.Val431Ile |
S175 |
15 | BAA04g08090 | A04 | 5503481 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Phe |
S207 |