Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17740 | A05 | 10022848 | G | A | missense_variant | MODERATE | c.2683C>T|p.Leu895Phe |
S297 |
2 | BAA05g17740 | A05 | 10023667 | G | A | synonymous_variant | LOW | c.2187C>T|p.His729His |
S200 |
3 | BAA05g17740 | A05 | 10024413 | C | T | synonymous_variant | LOW | c.1707G>A|p.Glu569Glu |
S232 |
4 | BAA05g17740 | A05 | 10024928 | C | T | missense_variant | MODERATE | c.1192G>A|p.Asp398Asn |
S259 |
5 | BAA05g17740 | A05 | 10025819 | G | A | intron_variant | MODIFIER | c.648-37C>T| |
S245 |
6 | BAA05g17740 | A05 | 10025900 | C | T | synonymous_variant | LOW | c.627G>A|p.Lys209Lys |
S100 |
7 | BAA05g17740 | A05 | 10026090 | G | A | missense_variant | MODERATE | c.511C>T|p.Pro171Ser |
S14 |
8 | BAA05g17740 | A05 | 10026390 | G | A | intron_variant | MODIFIER | c.310+58C>T| |
S303 |
9 | BAA05g17740 | A05 | 10027117 | G | A | upstream_gene_variant | MODIFIER | c.-120C>T| |
S7 |
10 | BAA05g17740 | A05 | 10028140 | C | T | upstream_gene_variant | MODIFIER | c.-1143G>A| |
S281 |
11 | BAA05g17740 | A05 | 10028760 | G | A | upstream_gene_variant | MODIFIER | c.-1763C>T| |
S308 |
12 | BAA05g17740 | A05 | 10029181 | C | T | upstream_gene_variant | MODIFIER | c.-2184G>A| |
S260 |
13 | BAA05g17740 | A05 | 10029261 | C | T | upstream_gene_variant | MODIFIER | c.-2264G>A| |
S198 |
14 | BAA05g17740 | A05 | 10029308 | G | A | upstream_gene_variant | MODIFIER | c.-2311C>T| |
S150 |
15 | BAA05g17740 | A05 | 10030723 | G | A | upstream_gene_variant | MODIFIER | c.-3726C>T| |
S282 |
16 | BAA05g17740 | A05 | 10031309 | C | T | upstream_gene_variant | MODIFIER | c.-4312G>A| |
S255 |