Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11790 | A10 | 13364111 | C | T | upstream_gene_variant | MODIFIER | c.-4804C>T| |
S143 |
2 | BAA10g11790 | A10 | 13365217 | C | T | upstream_gene_variant | MODIFIER | c.-3698C>T| |
S166 |
3 | BAA10g11790 | A10 | 13365824 | T | G | upstream_gene_variant | MODIFIER | c.-3091T>G| |
S127 S14 S151 S165 S295 S308 S4 S45 S53 |
4 | BAA10g11790 | A10 | 13367862 | C | T | upstream_gene_variant | MODIFIER | c.-1053C>T| |
S169 |
5 | BAA10g11790 | A10 | 13369845 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.312-1G>A| |
S45 |
6 | BAA10g11790 | A10 | 13370035 | G | A | missense_variant | MODERATE | c.501G>A|p.Met167Ile |
S278 |