Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g12190 | A05 | 6207852 | G | A | downstream_gene_variant | MODIFIER | c.*4883C>T| |
S238 |
2 | BAA05g12190 | A05 | 6208560 | G | A | downstream_gene_variant | MODIFIER | c.*4175C>T| |
S122 |
3 | BAA05g12190 | A05 | 6211075 | C | T | downstream_gene_variant | MODIFIER | c.*1660G>A| |
S130 |
4 | BAA05g12190 | A05 | 6212013 | G | A | downstream_gene_variant | MODIFIER | c.*722C>T| |
S45 |
5 | BAA05g12190 | A05 | 6212622 | C | T | downstream_gene_variant | MODIFIER | c.*113G>A| |
S79 |
6 | BAA05g12190 | A05 | 6212699 | G | A | downstream_gene_variant | MODIFIER | c.*36C>T| |
S178 |
7 | BAA05g12190 | A05 | 6212961 | C | T | intron_variant | MODIFIER | c.954+101G>A| |
S246 |
8 | BAA05g12190 | A05 | 6213201 | G | A | missense_variant | MODERATE | c.815C>T|p.Ala272Val |
S117 |
9 | BAA05g12190 | A05 | 6213284 | C | T | intron_variant | MODIFIER | c.747-15G>A| |
S61 |
10 | BAA05g12190 | A05 | 6214159 | C | T | missense_variant | MODERATE | c.365G>A|p.Gly122Glu |
S262 |
11 | BAA05g12190 | A05 | 6214504 | G | A | intron_variant | MODIFIER | c.334-314C>T| |
S4 |
12 | BAA05g12190 | A05 | 6214623 | G | A | intron_variant | MODIFIER | c.334-433C>T| |
S245 |
13 | BAA05g12190 | A05 | 6217692 | G | A | upstream_gene_variant | MODIFIER | c.-2146C>T| |
S294 |
14 | BAA05g12190 | A05 | 6218360 | A | T | upstream_gene_variant | MODIFIER | c.-2814T>A| |
S75 S81 |
15 | BAA05g12190 | A05 | 6218468 | G | A | upstream_gene_variant | MODIFIER | c.-2922C>T| |
S107 |
16 | BAA05g12190 | A05 | 6219502 | G | A | upstream_gene_variant | MODIFIER | c.-3956C>T| |
S192 |
17 | BAA05g12190 | A05 | 6220091 | G | A | upstream_gene_variant | MODIFIER | c.-4545C>T| |
S272 |
18 | BAA05g12190 | A05 | 6220124 | C | T | upstream_gene_variant | MODIFIER | c.-4578G>A| |
S256 |