Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41250 | A06 | 26855760 | G | A | synonymous_variant | LOW | c.1332C>T|p.Ile444Ile |
S41 |
2 | BAA06g41250 | A06 | 26855828 | C | T | missense_variant | MODERATE | c.1264G>A|p.Val422Ile |
S272 |
3 | BAA06g41250 | A06 | 26856037 | G | A | missense_variant | MODERATE | c.1055C>T|p.Ser352Leu |
S162 |
4 | BAA06g41250 | A06 | 26856206 | C | T | missense_variant | MODERATE | c.886G>A|p.Ala296Thr |
S10 |
5 | BAA06g41250 | A06 | 26856890 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.346-1G>A| |
S58 |
6 | BAA06g41250 | A06 | 26857376 | G | A | missense_variant | MODERATE | c.20C>T|p.Pro7Leu |
S50 |
7 | BAA06g41250 | A06 | 26857390 | C | T | synonymous_variant | LOW | c.6G>A|p.Gly2Gly |
S45 |
8 | BAA06g41250 | A06 | 26858475 | G | A | upstream_gene_variant | MODIFIER | c.-1080C>T| |
S229 |
9 | BAA06g41250 | A06 | 26858481 | C | T | upstream_gene_variant | MODIFIER | c.-1086G>A| |
S86 |