Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g40300 | A06 | 26211766 | G | A | missense_variant | MODERATE | c.583G>A|p.Glu195Lys |
S157 S80 |
2 | BAA06g40300 | A06 | 26213045 | C | T | missense_variant | MODERATE | c.1075C>T|p.Leu359Phe |
S108 |
3 | BAA06g40300 | A06 | 26213634 | C | T | splice_region_variant&intron_variant | LOW | c.1437+7C>T| |
S210 S225 |
4 | BAA06g40300 | A06 | 26214093 | G | A | synonymous_variant | LOW | c.1653G>A|p.Glu551Glu |
S73 S91 |
5 | BAA06g40300 | A06 | 26214153 | C | T | synonymous_variant | LOW | c.1713C>T|p.Phe571Phe |
S86 |
6 | BAA06g40300 | A06 | 26215465 | A | T | downstream_gene_variant | MODIFIER | c.*1261A>T| |
S123 |
7 | BAA06g40300 | A06 | 26216121 | T | G | downstream_gene_variant | MODIFIER | c.*1917T>G| |
S217 S248 S56 |
8 | BAA06g40300 | A06 | 26216435 | G | A | downstream_gene_variant | MODIFIER | c.*2231G>A| |
S161 |
9 | BAA06g40300 | A06 | 26218393 | G | A | downstream_gene_variant | MODIFIER | c.*4189G>A| |
S118 |