Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g18550 | A03 | 8204956 | G | A | missense_variant | MODERATE | c.1298C>T|p.Ala433Val |
S13 |
2 | BAA03g18550 | A03 | 8205681 | G | A | missense_variant | MODERATE | c.988C>T|p.Pro330Ser |
S174 S216 S241 S27 S39 |
3 | BAA03g18550 | A03 | 8206033 | C | T | missense_variant | MODERATE | c.820G>A|p.Gly274Arg |
S34 |
4 | BAA03g18550 | A03 | 8206250 | C | T | missense_variant | MODERATE | c.695G>A|p.Gly232Asp |
S173 S176 |
5 | BAA03g18550 | A03 | 8206492 | C | T | splice_region_variant&intron_variant | LOW | c.547-4G>A| |
S266 |
6 | BAA03g18550 | A03 | 8206756 | G | A | synonymous_variant | LOW | c.447C>T|p.Ala149Ala |
S255 |
7 | BAA03g18550 | A03 | 8207119 | G | A | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S33 |
8 | BAA03g18550 | A03 | 8207217 | G | A | intron_variant | MODIFIER | c.168-25C>T| |
S130 |
9 | BAA03g18550 | A03 | 8207331 | C | T | synonymous_variant | LOW | c.132G>A|p.Arg44Arg |
S263 |
10 | BAA03g18550 | A03 | 8207595 | C | T | intron_variant | MODIFIER | c.90+160G>A| |
S121 |
11 | BAA03g18550 | A03 | 8208881 | G | A | upstream_gene_variant | MODIFIER | c.-1037C>T| |
S274 |
12 | BAA03g18550 | A03 | 8208963 | C | T | upstream_gene_variant | MODIFIER | c.-1119G>A| |
S107 |
13 | BAA03g18550 | A03 | 8209135 | C | T | upstream_gene_variant | MODIFIER | c.-1291G>A| |
S70 |
14 | BAA03g18550 | A03 | 8210243 | G | A | upstream_gene_variant | MODIFIER | c.-2399C>T| |
S107 |
15 | BAA03g18550 | A03 | 8212165 | G | T | upstream_gene_variant | MODIFIER | c.-4321C>A| |
S144 |
16 | BAA03g18550 | A03 | 8212269 | G | A | upstream_gene_variant | MODIFIER | c.-4425C>T| |
S242 |