Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g22480 | A10 | 19296106 | C | T | missense_variant | MODERATE | c.13G>A|p.Val5Ile |
S40 S49 |
2 | BAA10g22480 | A10 | 19296183 | G | A | upstream_gene_variant | MODIFIER | c.-65C>T| |
S35 |
3 | BAA10g22480 | A10 | 19296239 | G | A | upstream_gene_variant | MODIFIER | c.-121C>T| |
S16 |
4 | BAA10g22480 | A10 | 19296709 | G | A | upstream_gene_variant | MODIFIER | c.-591C>T| |
S284 |
5 | BAA10g22480 | A10 | 19297189 | C | T | upstream_gene_variant | MODIFIER | c.-1071G>A| |
S33 |
6 | BAA10g22480 | A10 | 19297772 | C | T | upstream_gene_variant | MODIFIER | c.-1654G>A| |
S297 |
7 | BAA10g22480 | A10 | 19298250 | G | A | upstream_gene_variant | MODIFIER | c.-2132C>T| |
S62 |
8 | BAA10g22480 | A10 | 19300358 | G | A | upstream_gene_variant | MODIFIER | c.-4240C>T| |
S294 |
9 | BAA10g22480 | A10 | 19300533 | C | T | upstream_gene_variant | MODIFIER | c.-4415G>A| |
S206 S26 |