Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g10580 | A04 | 16679393 | G | A | splice_region_variant&intron_variant | LOW | c.1330-8C>T| |
S88 |
2 | BAA04g10580 | A04 | 16679556 | G | A | synonymous_variant | LOW | c.1251C>T|p.Asn417Asn |
S158 |
3 | BAA04g10580 | A04 | 16681764 | C | T | synonymous_variant | LOW | c.537G>A|p.Leu179Leu |
S30 S31 |
4 | BAA04g10580 | A04 | 16681785 | G | A | synonymous_variant | LOW | c.516C>T|p.Asp172Asp |
S61 |
5 | BAA04g10580 | A04 | 16682151 | C | T | stop_gained | HIGH | c.339G>A|p.Trp113* |
S89 |
6 | BAA04g10580 | A04 | 16682209 | C | T | missense_variant | MODERATE | c.281G>A|p.Ser94Asn |
S30 S31 |
7 | BAA04g10580 | A04 | 16682221 | C | G | missense_variant | MODERATE | c.269G>C|p.Ser90Thr |
S280 |
8 | BAA04g10580 | A04 | 16682810 | C | T | splice_donor_variant&intron_variant | HIGH | c.100+1G>A| |
S139 |
9 | BAA04g10580 | A04 | 16682837 | G | A | missense_variant | MODERATE | c.74C>T|p.Ser25Phe |
S259 |
10 | BAA04g10580 | A04 | 16683509 | C | T | upstream_gene_variant | MODIFIER | c.-599G>A| |
S185 |
11 | BAA04g10580 | A04 | 16683627 | C | T | upstream_gene_variant | MODIFIER | c.-717G>A| |
S37 |
12 | BAA04g10580 | A04 | 16683713 | C | T | upstream_gene_variant | MODIFIER | c.-803G>A| |
S192 |
13 | BAA04g10580 | A04 | 16683922 | C | T | upstream_gene_variant | MODIFIER | c.-1012G>A| |
S184 |
14 | BAA04g10580 | A04 | 16684665 | C | T | upstream_gene_variant | MODIFIER | c.-1755G>A| |
S297 |
15 | BAA04g10580 | A04 | 16685878 | G | A | upstream_gene_variant | MODIFIER | c.-2968C>T| |
S108 |
16 | BAA04g10580 | A04 | 16685888 | G | A | upstream_gene_variant | MODIFIER | c.-2978C>T| |
S201 |
17 | BAA04g10580 | A04 | 16686111 | C | T | upstream_gene_variant | MODIFIER | c.-3201G>A| |
S98 |
18 | BAA04g10580 | A04 | 16687135 | G | A | upstream_gene_variant | MODIFIER | c.-4225C>T| |
S56 |