Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g29900 | A03 | 13996876 | G | A | upstream_gene_variant | MODIFIER | c.-4483G>A| |
S122 |
2 | BAA03g29900 | A03 | 13997634 | G | A | upstream_gene_variant | MODIFIER | c.-3725G>A| |
S95 |
3 | BAA03g29900 | A03 | 13997854 | G | A | upstream_gene_variant | MODIFIER | c.-3505G>A| |
S206 S26 |
4 | BAA03g29900 | A03 | 13998599 | C | T | upstream_gene_variant | MODIFIER | c.-2760C>T| |
S87 |
5 | BAA03g29900 | A03 | 13999943 | G | A | upstream_gene_variant | MODIFIER | c.-1416G>A| |
S114 |
6 | BAA03g29900 | A03 | 14000184 | G | A | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S138 |
7 | BAA03g29900 | A03 | 14000922 | G | A | upstream_gene_variant | MODIFIER | c.-437G>A| |
S194 |
8 | BAA03g29900 | A03 | 14002698 | C | T | missense_variant | MODERATE | c.962C>T|p.Pro321Leu |
S299 |
9 | BAA03g29900 | A03 | 14002910 | G | A | missense_variant | MODERATE | c.1174G>A|p.Asp392Asn |
S13 |
10 | BAA03g29900 | A03 | 14003223 | C | T | splice_region_variant&intron_variant | LOW | c.1270-6C>T| |
S195 |
11 | BAA03g29900 | A03 | 14003276 | C | T | synonymous_variant | LOW | c.1317C>T|p.Pro439Pro |
S241 |
12 | BAA03g29900 | A03 | 14003558 | C | T | synonymous_variant | LOW | c.1599C>T|p.Ser533Ser |
S18 |
13 | BAA03g29900 | A03 | 14003561 | C | T | synonymous_variant | LOW | c.1602C>T|p.Leu534Leu |
S216 |
14 | BAA03g29900 | A03 | 14003811 | G | A | missense_variant | MODERATE | c.1852G>A|p.Ala618Thr |
S209 |
15 | BAA03g29900 | A03 | 14004802 | G | A | downstream_gene_variant | MODIFIER | c.*962G>A| |
S149 |
16 | BAA03g29900 | A03 | 14005996 | G | A | downstream_gene_variant | MODIFIER | c.*2156G>A| |
S185 |