Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g30150 | A08 | 20481212 | C | T | missense_variant | MODERATE | c.4507G>A|p.Gly1503Ser |
S228 |
2 | BAA08g30150 | A08 | 20481642 | C | T | synonymous_variant | LOW | c.4077G>A|p.Thr1359Thr |
S70 |
3 | BAA08g30150 | A08 | 20483255 | G | A | stop_gained | HIGH | c.3070C>T|p.Arg1024* |
S30 S31 |
4 | BAA08g30150 | A08 | 20484773 | C | T | missense_variant | MODERATE | c.1936G>A|p.Gly646Ser |
S42 |
5 | BAA08g30150 | A08 | 20485220 | C | T | missense_variant | MODERATE | c.1489G>A|p.Gly497Arg |
S230 |
6 | BAA08g30150 | A08 | 20485684 | G | A | missense_variant&splice_region_variant | MODERATE | c.1025C>T|p.Ser342Leu |
S256 |
7 | BAA08g30150 | A08 | 20485804 | G | A | missense_variant | MODERATE | c.1016C>T|p.Ser339Phe |
S238 |
8 | BAA08g30150 | A08 | 20485866 | C | T | synonymous_variant | LOW | c.954G>A|p.Gly318Gly |
S296 |
9 | BAA08g30150 | A08 | 20486386 | G | A | missense_variant | MODERATE | c.584C>T|p.Ser195Leu |
S187 |
10 | BAA08g30150 | A08 | 20487319 | C | T | synonymous_variant | LOW | c.84G>A|p.Gln28Gln |
S94 |
11 | BAA08g30150 | A08 | 20488036 | G | A | upstream_gene_variant | MODIFIER | c.-634C>T| |
S96 |
12 | BAA08g30150 | A08 | 20488078 | C | T | upstream_gene_variant | MODIFIER | c.-676G>A| |
S294 |
13 | BAA08g30150 | A08 | 20488930 | G | A | upstream_gene_variant | MODIFIER | c.-1528C>T| |
S195 |
14 | BAA08g30150 | A08 | 20488962 | G | A | upstream_gene_variant | MODIFIER | c.-1560C>T| |
S247 |
15 | BAA08g30150 | A08 | 20490727 | G | A | upstream_gene_variant | MODIFIER | c.-3325C>T| |
S282 |
16 | BAA08g30150 | A08 | 20492233 | C | T | upstream_gene_variant | MODIFIER | c.-4831G>A| |
S176 S94 |