Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g20820 | A08 | 15938077 | C | T | missense_variant | MODERATE | c.1937G>A|p.Gly646Glu |
S206 S26 |
2 | BAA08g20820 | A08 | 15938220 | C | T | synonymous_variant | LOW | c.1794G>A|p.Lys598Lys |
S1 S90 |
3 | BAA08g20820 | A08 | 15938601 | C | T | missense_variant | MODERATE | c.1498G>A|p.Asp500Asn |
S249 |
4 | BAA08g20820 | A08 | 15939159 | C | T | splice_donor_variant&intron_variant | HIGH | c.1151+1G>A| |
S58 |
5 | BAA08g20820 | A08 | 15939616 | G | A | missense_variant | MODERATE | c.872C>T|p.Ser291Phe |
S287 |
6 | BAA08g20820 | A08 | 15940370 | G | A | missense_variant | MODERATE | c.292C>T|p.Pro98Ser |
S125 |
7 | BAA08g20820 | A08 | 15940378 | C | T | missense_variant | MODERATE | c.284G>A|p.Gly95Glu |
S251 |
8 | BAA08g20820 | A08 | 15940511 | C | T | missense_variant | MODERATE | c.151G>A|p.Ala51Thr |
S223 |
9 | BAA08g20820 | A08 | 15940647 | G | A | synonymous_variant | LOW | c.15C>T|p.Ala5Ala |
S292 |
10 | BAA08g20820 | A08 | 15940980 | C | T | upstream_gene_variant | MODIFIER | c.-319G>A| |
S19 |
11 | BAA08g20820 | A08 | 15941142 | C | T | upstream_gene_variant | MODIFIER | c.-481G>A| |
S186 S23 |
12 | BAA08g20820 | A08 | 15941625 | C | T | upstream_gene_variant | MODIFIER | c.-964G>A| |
S110 |
13 | BAA08g20820 | A08 | 15942108 | G | A | upstream_gene_variant | MODIFIER | c.-1447C>T| |
S205 |
14 | BAA08g20820 | A08 | 15942509 | C | T | upstream_gene_variant | MODIFIER | c.-1848G>A| |
S149 |
15 | BAA08g20820 | A08 | 15943867 | C | T | upstream_gene_variant | MODIFIER | c.-3206G>A| |
S192 |
16 | BAA08g20820 | A08 | 15944014 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S265 |