Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20580 | A10 | 18443936 | G | A | upstream_gene_variant | MODIFIER | c.-4607G>A| |
S163 |
2 | BAA10g20580 | A10 | 18444322 | C | T | upstream_gene_variant | MODIFIER | c.-4221C>T| |
S168 |
3 | BAA10g20580 | A10 | 18445223 | G | A | upstream_gene_variant | MODIFIER | c.-3320G>A| |
S226 S41 |
4 | BAA10g20580 | A10 | 18445497 | C | T | upstream_gene_variant | MODIFIER | c.-3046C>T| |
S2 |
5 | BAA10g20580 | A10 | 18445889 | C | T | upstream_gene_variant | MODIFIER | c.-2654C>T| |
S70 |
6 | BAA10g20580 | A10 | 18446764 | G | A | upstream_gene_variant | MODIFIER | c.-1779G>A| |
S105 S106 |
7 | BAA10g20580 | A10 | 18447057 | C | T | upstream_gene_variant | MODIFIER | c.-1486C>T| |
S221 |
8 | BAA10g20580 | A10 | 18448209 | G | A | upstream_gene_variant | MODIFIER | c.-334G>A| |
S172 S217 |
9 | BAA10g20580 | A10 | 18448972 | C | T | missense_variant | MODERATE | c.302C>T|p.Ser101Phe |
S46 |