Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17590 | A09 | 10518722 | C | T | missense_variant | MODERATE | c.1160G>A|p.Gly387Asp |
S15 S3 |
2 | BAA09g17590 | A09 | 10519235 | G | A | stop_gained | HIGH | c.853C>T|p.Arg285* |
S262 |
3 | BAA09g17590 | A09 | 10520672 | C | T | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S132 S137 S215 S89 |
4 | BAA09g17590 | A09 | 10522310 | G | A | upstream_gene_variant | MODIFIER | c.-731C>T| |
S79 S84 |
5 | BAA09g17590 | A09 | 10522473 | C | T | upstream_gene_variant | MODIFIER | c.-894G>A| |
S133 |
6 | BAA09g17590 | A09 | 10522500 | G | A | upstream_gene_variant | MODIFIER | c.-921C>T| |
S245 |
7 | BAA09g17590 | A09 | 10523122 | C | T | upstream_gene_variant | MODIFIER | c.-1543G>A| |
S16 S181 S217 S248 S56 |
8 | BAA09g17590 | A09 | 10524003 | C | T | upstream_gene_variant | MODIFIER | c.-2424G>A| |
S132 S137 S215 S89 |
9 | BAA09g17590 | A09 | 10525284 | G | A | upstream_gene_variant | MODIFIER | c.-3705C>T| |
S66 |
10 | BAA09g17590 | A09 | 10525942 | G | A | upstream_gene_variant | MODIFIER | c.-4363C>T| |
S79 S84 |
11 | BAA09g17590 | A09 | 10526252 | C | T | upstream_gene_variant | MODIFIER | c.-4673G>A| |
S305 |
12 | BAA09g17590 | A09 | 10526303 | C | T | upstream_gene_variant | MODIFIER | c.-4724G>A| |
S237 |
13 | BAA09g17590 | A09 | 10526544 | G | A | upstream_gene_variant | MODIFIER | c.-4965C>T| |
S216 |