Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01560 | A06 | 991492 | A | G | downstream_gene_variant | MODIFIER | c.*3530T>C| |
S280 |
2 | BAA06g01560 | A06 | 991838 | G | A | downstream_gene_variant | MODIFIER | c.*3184C>T| |
S217 S248 |
3 | BAA06g01560 | A06 | 993560 | C | T | downstream_gene_variant | MODIFIER | c.*1462G>A| |
S53 |
4 | BAA06g01560 | A06 | 994326 | C | T | downstream_gene_variant | MODIFIER | c.*696G>A| |
S221 |
5 | BAA06g01560 | A06 | 994669 | G | A | downstream_gene_variant | MODIFIER | c.*353C>T| |
S244 |
6 | BAA06g01560 | A06 | 994931 | G | A | downstream_gene_variant | MODIFIER | c.*91C>T| |
S122 |
7 | BAA06g01560 | A06 | 995792 | C | T | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S195 |
8 | BAA06g01560 | A06 | 999436 | C | T | upstream_gene_variant | MODIFIER | c.-3596G>A| |
S42 |
9 | BAA06g01560 | A06 | 999902 | C | T | upstream_gene_variant | MODIFIER | c.-4062G>A| |
S185 |