Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47000 | A09 | 51501561 | G | A | missense_variant | MODERATE | c.109G>A|p.Glu37Lys |
S264 |
2 | BAA09g47000 | A09 | 51501677 | C | T | synonymous_variant | LOW | c.225C>T|p.Leu75Leu |
S278 |
3 | BAA09g47000 | A09 | 51502046 | G | A | synonymous_variant | LOW | c.594G>A|p.Arg198Arg |
S231 |
4 | BAA09g47000 | A09 | 51503355 | G | A | intron_variant | MODIFIER | c.619-588G>A| |
S133 |
5 | BAA09g47000 | A09 | 51503975 | G | A | synonymous_variant | LOW | c.651G>A|p.Glu217Glu |
S308 |
6 | BAA09g47000 | A09 | 51504364 | G | A | synonymous_variant | LOW | c.966G>A|p.Lys322Lys |
S266 |
7 | BAA09g47000 | A09 | 51504395 | G | A | missense_variant | MODERATE | c.997G>A|p.Glu333Lys |
S116 |
8 | BAA09g47000 | A09 | 51504423 | C | T | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S68 |
9 | BAA09g47000 | A09 | 51504580 | G | A | synonymous_variant | LOW | c.1182G>A|p.Gly394Gly |
S23 |
10 | BAA09g47000 | A09 | 51504665 | C | T | missense_variant | MODERATE | c.1267C>T|p.Arg423Cys |
S77 S82 |
11 | BAA09g47000 | A09 | 51504693 | C | T | missense_variant | MODERATE | c.1295C>T|p.Ser432Phe |
S58 |
12 | BAA09g47000 | A09 | 51505089 | G | A | missense_variant | MODERATE | c.1615G>A|p.Glu539Lys |
S274 |
13 | BAA09g47000 | A09 | 51505289 | G | A | missense_variant | MODERATE | c.1815G>A|p.Met605Ile |
S86 |
14 | BAA09g47000 | A09 | 51505622 | C | T | synonymous_variant | LOW | c.2148C>T|p.Ile716Ile |
S155 S211 |
15 | BAA09g47000 | A09 | 51505795 | C | T | missense_variant | MODERATE | c.2321C>T|p.Ala774Val |
S81 S85 |
16 | BAA09g47000 | A09 | 51505830 | C | T | missense_variant | MODERATE | c.2356C>T|p.Pro786Ser |
S144 |
17 | BAA09g47000 | A09 | 51506068 | C | T | missense_variant | MODERATE | c.2594C>T|p.Thr865Ile |
S30 S31 |
18 | BAA09g47000 | A09 | 51506154 | G | A | missense_variant | MODERATE | c.2680G>A|p.Glu894Lys |
S284 |
19 | BAA09g47000 | A09 | 51506473 | C | T | downstream_gene_variant | MODIFIER | c.*314C>T| |
S192 |