Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g07370 | A01 | 3257462 | G | A | upstream_gene_variant | MODIFIER | c.-4465G>A| |
S298 |
2 | BAA01g07370 | A01 | 3258050 | C | T | upstream_gene_variant | MODIFIER | c.-3877C>T| |
S244 |
3 | BAA01g07370 | A01 | 3258506 | C | T | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S150 |
4 | BAA01g07370 | A01 | 3260147 | C | T | upstream_gene_variant | MODIFIER | c.-1780C>T| |
S282 |
5 | BAA01g07370 | A01 | 3260184 | G | A | upstream_gene_variant | MODIFIER | c.-1743G>A| |
S12 |
6 | BAA01g07370 | A01 | 3260323 | G | A | upstream_gene_variant | MODIFIER | c.-1604G>A| |
S103 |
7 | BAA01g07370 | A01 | 3261222 | C | T | upstream_gene_variant | MODIFIER | c.-705C>T| |
S133 |
8 | BAA01g07370 | A01 | 3261421 | C | T | upstream_gene_variant | MODIFIER | c.-506C>T| |
S45 |
9 | BAA01g07370 | A01 | 3261737 | G | A | upstream_gene_variant | MODIFIER | c.-190G>A| |
S170 |
10 | BAA01g07370 | A01 | 3262304 | C | T | synonymous_variant | LOW | c.378C>T|p.Leu126Leu |
S18 |
11 | BAA01g07370 | A01 | 3262825 | G | A | missense_variant | MODERATE | c.542G>A|p.Gly181Asp |
S79 S91 |
12 | BAA01g07370 | A01 | 3263043 | C | T | missense_variant | MODERATE | c.760C>T|p.Leu254Phe |
S61 |
13 | BAA01g07370 | A01 | 3263222 | G | A | synonymous_variant | LOW | c.939G>A|p.Ser313Ser |
S45 |
14 | BAA01g07370 | A01 | 3263376 | C | T | intron_variant | MODIFIER | c.976+117C>T| |
S20 |
15 | BAA01g07370 | A01 | 3263544 | C | T | intron_variant | MODIFIER | c.976+285C>T| |
S296 |
16 | BAA01g07370 | A01 | 3264442 | C | T | downstream_gene_variant | MODIFIER | c.*353C>T| |
S250 |
17 | BAA01g07370 | A01 | 3265141 | G | A | downstream_gene_variant | MODIFIER | c.*1052G>A| |
S17 |