Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39730 | A01 | 26379116 | C | T | upstream_gene_variant | MODIFIER | c.-4549C>T| |
S201 |
2 | BAA01g39730 | A01 | 26380623 | G | A | upstream_gene_variant | MODIFIER | c.-3042G>A| |
S278 |
3 | BAA01g39730 | A01 | 26380978 | C | T | upstream_gene_variant | MODIFIER | c.-2687C>T| |
S56 |
4 | BAA01g39730 | A01 | 26380996 | G | A | upstream_gene_variant | MODIFIER | c.-2669G>A| |
S246 |
5 | BAA01g39730 | A01 | 26382114 | C | T | upstream_gene_variant | MODIFIER | c.-1551C>T| |
S282 |
6 | BAA01g39730 | A01 | 26382934 | C | T | upstream_gene_variant | MODIFIER | c.-731C>T| |
S278 |
7 | BAA01g39730 | A01 | 26383071 | G | A | upstream_gene_variant | MODIFIER | c.-594G>A| |
S196 |
8 | BAA01g39730 | A01 | 26383190 | G | A | upstream_gene_variant | MODIFIER | c.-475G>A| |
S262 |
9 | BAA01g39730 | A01 | 26383858 | C | T | missense_variant | MODERATE | c.194C>T|p.Ala65Val |
S165 |
10 | BAA01g39730 | A01 | 26385437 | G | A | downstream_gene_variant | MODIFIER | c.*723G>A| |
S76 |
11 | BAA01g39730 | A01 | 26387823 | C | T | downstream_gene_variant | MODIFIER | c.*3109C>T| |
S50 |
12 | BAA01g39730 | A01 | 26388114 | C | T | downstream_gene_variant | MODIFIER | c.*3400C>T| |
S200 |
13 | BAA01g39730 | A01 | 26388900 | G | A | downstream_gene_variant | MODIFIER | c.*4186G>A| |
S143 |
14 | BAA01g39730 | A01 | 26389578 | A | G | downstream_gene_variant | MODIFIER | c.*4864A>G| |
S216 |