Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00090 | A08 | 80220 | G | A | upstream_gene_variant | MODIFIER | c.-2604G>A| |
S229 |
2 | BAA08g00090 | A08 | 81145 | G | A | upstream_gene_variant | MODIFIER | c.-1679G>A| |
S35 |
3 | BAA08g00090 | A08 | 81571 | G | A | upstream_gene_variant | MODIFIER | c.-1253G>A| |
S5 |
4 | BAA08g00090 | A08 | 81745 | C | T | upstream_gene_variant | MODIFIER | c.-1079C>T| |
S288 |
5 | BAA08g00090 | A08 | 81933 | C | T | upstream_gene_variant | MODIFIER | c.-891C>T| |
S55 |
6 | BAA08g00090 | A08 | 81986 | G | A | upstream_gene_variant | MODIFIER | c.-838G>A| |
S221 |
7 | BAA08g00090 | A08 | 82320 | C | T | upstream_gene_variant | MODIFIER | c.-504C>T| |
S78 |
8 | BAA08g00090 | A08 | 82917 | G | A | missense_variant | MODERATE | c.94G>A|p.Gly32Arg |
S69 |
9 | BAA08g00090 | A08 | 86182 | G | A | missense_variant | MODERATE | c.1390G>A|p.Ala464Thr |
S200 |
10 | BAA08g00090 | A08 | 86442 | C | T | splice_region_variant&intron_variant | LOW | c.1647+3C>T| |
S135 |
11 | BAA08g00090 | A08 | 87769 | C | T | missense_variant | MODERATE | c.2539C>T|p.His847Tyr |
S159 S243 |