Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g23050 | A10 | 19580929 | C | T | missense_variant | MODERATE | c.179G>A|p.Gly60Glu |
S276 |
2 | BAA10g23050 | A10 | 19581426 | G | A | upstream_gene_variant | MODIFIER | c.-253C>T| |
S280 |
3 | BAA10g23050 | A10 | 19581743 | C | T | upstream_gene_variant | MODIFIER | c.-570G>A| |
S130 |
4 | BAA10g23050 | A10 | 19583378 | C | T | upstream_gene_variant | MODIFIER | c.-2205G>A| |
S177 |
5 | BAA10g23050 | A10 | 19583397 | G | A | upstream_gene_variant | MODIFIER | c.-2224C>T| |
S192 |
6 | BAA10g23050 | A10 | 19583850 | G | A | upstream_gene_variant | MODIFIER | c.-2677C>T| |
S288 |
7 | BAA10g23050 | A10 | 19584462 | C | T | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S108 |
8 | BAA10g23050 | A10 | 19584880 | G | A | upstream_gene_variant | MODIFIER | c.-3707C>T| |
S128 |
9 | BAA10g23050 | A10 | 19585415 | G | A | upstream_gene_variant | MODIFIER | c.-4242C>T| |
S18 |