Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g06660 | A07 | 16026688 | C | T | missense_variant | MODERATE | c.2884G>A|p.Ala962Thr |
S296 |
2 | BAA07g06660 | A07 | 16026934 | G | A | missense_variant | MODERATE | c.2723C>T|p.Ser908Phe |
S241 |
3 | BAA07g06660 | A07 | 16026986 | C | T | missense_variant | MODERATE | c.2671G>A|p.Glu891Lys |
S276 |
4 | BAA07g06660 | A07 | 16027346 | C | T | splice_donor_variant&intron_variant | HIGH | c.2523+1G>A| |
S303 |
5 | BAA07g06660 | A07 | 16028955 | C | T | missense_variant | MODERATE | c.1753G>A|p.Gly585Arg |
S152 |
6 | BAA07g06660 | A07 | 16029157 | C | T | synonymous_variant | LOW | c.1620G>A|p.Lys540Lys |
S297 |
7 | BAA07g06660 | A07 | 16029754 | C | T | synonymous_variant | LOW | c.1023G>A|p.Arg341Arg |
S216 |
8 | BAA07g06660 | A07 | 16030855 | C | T | missense_variant | MODERATE | c.193G>A|p.Ala65Thr |
S37 |
9 | BAA07g06660 | A07 | 16031361 | G | A | upstream_gene_variant | MODIFIER | c.-29C>T| |
S46 |
10 | BAA07g06660 | A07 | 16031934 | C | T | upstream_gene_variant | MODIFIER | c.-602G>A| |
S238 |
11 | BAA07g06660 | A07 | 16032079 | C | T | upstream_gene_variant | MODIFIER | c.-747G>A| |
S181 |
12 | BAA07g06660 | A07 | 16033203 | G | A | upstream_gene_variant | MODIFIER | c.-1871C>T| |
S122 |
13 | BAA07g06660 | A07 | 16033206 | C | T | upstream_gene_variant | MODIFIER | c.-1874G>A| |
S221 |
14 | BAA07g06660 | A07 | 16033721 | C | T | upstream_gene_variant | MODIFIER | c.-2389G>A| |
S286 |
15 | BAA07g06660 | A07 | 16035413 | C | T | upstream_gene_variant | MODIFIER | c.-4081G>A| |
S281 |
16 | BAA07g06660 | A07 | 16036073 | C | T | upstream_gene_variant | MODIFIER | c.-4741G>A| |
S255 |
17 | BAA07g06660 | A07 | 16036120 | C | T | upstream_gene_variant | MODIFIER | c.-4788G>A| |
S150 |
18 | BAA07g06660 | A07 | 16036269 | C | T | upstream_gene_variant | MODIFIER | c.-4937G>A| |
S127 |