Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00740 | A06 | 533464 | C | T | missense_variant | MODERATE | c.1094G>A|p.Arg365His |
S188 |
2 | BAA06g00740 | A06 | 533912 | C | T | missense_variant | MODERATE | c.646G>A|p.Gly216Arg |
S274 |
3 | BAA06g00740 | A06 | 533955 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.604-1G>A| |
S62 |
4 | BAA06g00740 | A06 | 534316 | G | A | missense_variant | MODERATE | c.514C>T|p.Leu172Phe |
S115 |
5 | BAA06g00740 | A06 | 537280 | G | A | upstream_gene_variant | MODIFIER | c.-2295C>T| |
S286 |
6 | BAA06g00740 | A06 | 537546 | C | A | upstream_gene_variant | MODIFIER | c.-2561G>T| |
S305 |