Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32200 | A02 | 27116169 | C | T | upstream_gene_variant | MODIFIER | c.-4975C>T| |
S218 |
2 | BAA02g32200 | A02 | 27116929 | C | T | upstream_gene_variant | MODIFIER | c.-4215C>T| |
S120 |
3 | BAA02g32200 | A02 | 27117106 | C | T | upstream_gene_variant | MODIFIER | c.-4038C>T| |
S162 |
4 | BAA02g32200 | A02 | 27117217 | C | T | upstream_gene_variant | MODIFIER | c.-3927C>T| |
S87 |
5 | BAA02g32200 | A02 | 27117459 | G | A | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S217 S248 |
6 | BAA02g32200 | A02 | 27119524 | G | A | upstream_gene_variant | MODIFIER | c.-1620G>A| |
S166 |
7 | BAA02g32200 | A02 | 27119632 | G | A | upstream_gene_variant | MODIFIER | c.-1512G>A| |
S281 |
8 | BAA02g32200 | A02 | 27119889 | C | T | upstream_gene_variant | MODIFIER | c.-1255C>T| |
S51 |
9 | BAA02g32200 | A02 | 27120971 | C | T | upstream_gene_variant | MODIFIER | c.-173C>T| |
S183 S198 |
10 | BAA02g32200 | A02 | 27121268 | C | T | intron_variant | MODIFIER | c.100+25C>T| |
S18 |
11 | BAA02g32200 | A02 | 27121834 | G | A | intron_variant | MODIFIER | c.377+240G>A| |
S148 S210 S30 S31 |
12 | BAA02g32200 | A02 | 27122204 | C | T | intron_variant | MODIFIER | c.377+610C>T| |
S114 |
13 | BAA02g32200 | A02 | 27122259 | C | T | intron_variant | MODIFIER | c.377+665C>T| |
S79 S91 |
14 | BAA02g32200 | A02 | 27122859 | G | A | intron_variant | MODIFIER | c.377+1265G>A| |
S247 |
15 | BAA02g32200 | A02 | 27123547 | C | T | intron_variant | MODIFIER | c.378-733C>T| |
S295 |
16 | BAA02g32200 | A02 | 27123732 | G | A | intron_variant | MODIFIER | c.378-548G>A| |
S69 |
17 | BAA02g32200 | A02 | 27124629 | C | A | missense_variant | MODERATE | c.630C>A|p.His210Gln |
S292 |
18 | BAA02g32200 | A02 | 27126007 | C | T | missense_variant | MODERATE | c.1348C>T|p.Leu450Phe |
S64 |
19 | BAA02g32200 | A02 | 27126070 | G | A | missense_variant | MODERATE | c.1411G>A|p.Gly471Arg |
S103 |
20 | BAA02g32200 | A02 | 27126228 | C | T | synonymous_variant | LOW | c.1569C>T|p.Val523Val |
S116 S34 |