Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19190 | A05 | 11231139 | G | A | upstream_gene_variant | MODIFIER | c.-4753G>A| |
S176 |
2 | BAA05g19190 | A05 | 11231934 | C | T | upstream_gene_variant | MODIFIER | c.-3958C>T| |
S146 |
3 | BAA05g19190 | A05 | 11231951 | G | A | upstream_gene_variant | MODIFIER | c.-3941G>A| |
S76 |
4 | BAA05g19190 | A05 | 11232384 | C | T | upstream_gene_variant | MODIFIER | c.-3508C>T| |
S20 |
5 | BAA05g19190 | A05 | 11233277 | C | T | upstream_gene_variant | MODIFIER | c.-2615C>T| |
S162 |
6 | BAA05g19190 | A05 | 11234580 | G | A | upstream_gene_variant | MODIFIER | c.-1312G>A| |
S156 |
7 | BAA05g19190 | A05 | 11234698 | G | A | upstream_gene_variant | MODIFIER | c.-1194G>A| |
S257 |
8 | BAA05g19190 | A05 | 11235432 | G | A | upstream_gene_variant | MODIFIER | c.-460G>A| |
S3 |
9 | BAA05g19190 | A05 | 11235560 | C | T | upstream_gene_variant | MODIFIER | c.-332C>T| |
S137 S215 |
10 | BAA05g19190 | A05 | 11235945 | C | T | synonymous_variant | LOW | c.54C>T|p.Asn18Asn |
S153 S213 S36 |
11 | BAA05g19190 | A05 | 11236233 | C | T | synonymous_variant | LOW | c.342C>T|p.Ser114Ser |
S271 |
12 | BAA05g19190 | A05 | 11236417 | C | T | missense_variant | MODERATE | c.526C>T|p.Pro176Ser |
S43 |
13 | BAA05g19190 | A05 | 11236442 | G | A | missense_variant | MODERATE | c.551G>A|p.Arg184Lys |
S246 |
14 | BAA05g19190 | A05 | 11237518 | G | A | stop_gained | HIGH | c.816G>A|p.Trp272* |
S301 S304 |
15 | BAA05g19190 | A05 | 11237584 | G | A | synonymous_variant | LOW | c.882G>A|p.Lys294Lys |
S288 |
16 | BAA05g19190 | A05 | 11240203 | C | T | downstream_gene_variant | MODIFIER | c.*2475C>T| |
S188 |