Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19980 | A09 | 12311586 | G | A | synonymous_variant | LOW | c.2379C>T|p.Arg793Arg |
S180 |
2 | BAA09g19980 | A09 | 12312083 | G | A | missense_variant | MODERATE | c.1882C>T|p.Pro628Ser |
S192 |
3 | BAA09g19980 | A09 | 12312345 | G | A | synonymous_variant | LOW | c.1620C>T|p.Asp540Asp |
S122 |
4 | BAA09g19980 | A09 | 12312699 | G | A | synonymous_variant | LOW | c.1266C>T|p.Asn422Asn |
S16 |
5 | BAA09g19980 | A09 | 12314175 | C | T | missense_variant | MODERATE | c.613G>A|p.Ala205Thr |
S85 |
6 | BAA09g19980 | A09 | 12314558 | G | A | missense_variant | MODERATE | c.230C>T|p.Ser77Phe |
S135 S152 S185 S273 S68 |
7 | BAA09g19980 | A09 | 12314729 | G | A | missense_variant | MODERATE | c.59C>T|p.Pro20Leu |
S149 |
8 | BAA09g19980 | A09 | 12315506 | G | A | upstream_gene_variant | MODIFIER | c.-719C>T| |
S207 |
9 | BAA09g19980 | A09 | 12315610 | G | A | upstream_gene_variant | MODIFIER | c.-823C>T| |
S40 S49 |
10 | BAA09g19980 | A09 | 12316887 | G | A | upstream_gene_variant | MODIFIER | c.-2100C>T| |
S79 S91 |
11 | BAA09g19980 | A09 | 12316921 | C | T | upstream_gene_variant | MODIFIER | c.-2134G>A| |
S273 |
12 | BAA09g19980 | A09 | 12317682 | G | A | upstream_gene_variant | MODIFIER | c.-2895C>T| |
S105 S106 |
13 | BAA09g19980 | A09 | 12317919 | C | T | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S270 |
14 | BAA09g19980 | A09 | 12318379 | G | A | upstream_gene_variant | MODIFIER | c.-3592C>T| |
S162 |
15 | BAA09g19980 | A09 | 12318752 | C | T | upstream_gene_variant | MODIFIER | c.-3965G>A| |
S263 |
16 | BAA09g19980 | A09 | 12318857 | G | A | upstream_gene_variant | MODIFIER | c.-4070C>T| |
S266 |
17 | BAA09g19980 | A09 | 12319506 | G | A | upstream_gene_variant | MODIFIER | c.-4719C>T| |
S82 S83 S88 S92 |