Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g06520 | A08 | 5271572 | C | T | downstream_gene_variant | MODIFIER | c.*4439G>A| |
S12 |
2 | BAA08g06520 | A08 | 5271777 | G | A | downstream_gene_variant | MODIFIER | c.*4234C>T| |
S246 |
3 | BAA08g06520 | A08 | 5271942 | C | T | downstream_gene_variant | MODIFIER | c.*4069G>A| |
S279 |
4 | BAA08g06520 | A08 | 5276134 | G | A | splice_region_variant&intron_variant | LOW | c.2247+4C>T| |
S204 |
5 | BAA08g06520 | A08 | 5276331 | G | A | missense_variant | MODERATE | c.2054C>T|p.Thr685Ile |
S87 |
6 | BAA08g06520 | A08 | 5276556 | G | A | missense_variant | MODERATE | c.1829C>T|p.Ser610Phe |
S130 |
7 | BAA08g06520 | A08 | 5278489 | C | T | missense_variant | MODERATE | c.517G>A|p.Ala173Thr |
S179 |
8 | BAA08g06520 | A08 | 5278714 | C | T | missense_variant | MODERATE | c.292G>A|p.Ala98Thr |
S226 |
9 | BAA08g06520 | A08 | 5279452 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S1 |
10 | BAA08g06520 | A08 | 5279722 | C | T | upstream_gene_variant | MODIFIER | c.-717G>A| |
S308 |
11 | BAA08g06520 | A08 | 5279832 | G | A | upstream_gene_variant | MODIFIER | c.-827C>T| |
S115 |
12 | BAA08g06520 | A08 | 5280078 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S185 |
13 | BAA08g06520 | A08 | 5280228 | C | T | upstream_gene_variant | MODIFIER | c.-1223G>A| |
S284 |