Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32220 | A01 | 21137979 | C | T | missense_variant | MODERATE | c.3661G>A|p.Glu1221Lys |
S233 |
2 | BAA01g32220 | A01 | 21138983 | C | T | missense_variant&splice_region_variant | MODERATE | c.2728G>A|p.Val910Ile |
S213 |
3 | BAA01g32220 | A01 | 21139642 | G | A | missense_variant | MODERATE | c.2231C>T|p.Ser744Phe |
S181 |
4 | BAA01g32220 | A01 | 21139732 | C | T | missense_variant | MODERATE | c.2141G>A|p.Arg714Lys |
S208 S93 |
5 | BAA01g32220 | A01 | 21140088 | C | T | synonymous_variant | LOW | c.1785G>A|p.Glu595Glu |
S53 |
6 | BAA01g32220 | A01 | 21140117 | C | T | missense_variant | MODERATE | c.1756G>A|p.Asp586Asn |
S192 |
7 | BAA01g32220 | A01 | 21140214 | G | A | synonymous_variant | LOW | c.1659C>T|p.Ala553Ala |
S260 |
8 | BAA01g32220 | A01 | 21140580 | C | T | splice_donor_variant&intron_variant | HIGH | c.1365+1G>A| |
S150 |
9 | BAA01g32220 | A01 | 21140808 | C | T | missense_variant | MODERATE | c.1216G>A|p.Ala406Thr |
S256 |
10 | BAA01g32220 | A01 | 21141951 | G | A | missense_variant | MODERATE | c.770C>T|p.Ser257Phe |
S302 |
11 | BAA01g32220 | A01 | 21143121 | G | A | missense_variant | MODERATE | c.187C>T|p.Pro63Ser |
S257 |
12 | BAA01g32220 | A01 | 21145877 | G | A | upstream_gene_variant | MODIFIER | c.-2570C>T| |
S172 S217 |
13 | BAA01g32220 | A01 | 21146207 | G | A | upstream_gene_variant | MODIFIER | c.-2900C>T| |
S221 |
14 | BAA01g32220 | A01 | 21146245 | C | T | upstream_gene_variant | MODIFIER | c.-2938G>A| |
S136 |
15 | BAA01g32220 | A01 | 21147795 | C | T | upstream_gene_variant | MODIFIER | c.-4488G>A| |
S48 |