Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g01700 | A04 | 985792 | C | T | downstream_gene_variant | MODIFIER | c.*1945G>A| |
S18 |
2 | BAA04g01700 | A04 | 986034 | C | T | downstream_gene_variant | MODIFIER | c.*1703G>A| |
S139 |
3 | BAA04g01700 | A04 | 986267 | G | A | downstream_gene_variant | MODIFIER | c.*1470C>T| |
S171 |
4 | BAA04g01700 | A04 | 986332 | C | T | downstream_gene_variant | MODIFIER | c.*1405G>A| |
S257 |
5 | BAA04g01700 | A04 | 986343 | G | A | downstream_gene_variant | MODIFIER | c.*1394C>T| |
S36 |
6 | BAA04g01700 | A04 | 986515 | G | A | downstream_gene_variant | MODIFIER | c.*1222C>T| |
S207 |
7 | BAA04g01700 | A04 | 986726 | C | T | downstream_gene_variant | MODIFIER | c.*1011G>A| |
S172 S217 |
8 | BAA04g01700 | A04 | 987187 | G | A | downstream_gene_variant | MODIFIER | c.*550C>T| |
S112 |
9 | BAA04g01700 | A04 | 988102 | C | T | missense_variant | MODERATE | c.838G>A|p.Val280Ile |
S292 |
10 | BAA04g01700 | A04 | 988933 | G | A | missense_variant | MODERATE | c.160C>T|p.Leu54Phe |
S183 S198 |
11 | BAA04g01700 | A04 | 991809 | C | T | upstream_gene_variant | MODIFIER | c.-2717G>A| |
S118 |
12 | BAA04g01700 | A04 | 992020 | G | A | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S251 |
13 | BAA04g01700 | A04 | 992284 | C | T | upstream_gene_variant | MODIFIER | c.-3192G>A| |
S9 |
14 | BAA04g01700 | A04 | 993121 | C | T | upstream_gene_variant | MODIFIER | c.-4029G>A| |
S180 |
15 | BAA04g01700 | A04 | 994065 | C | T | upstream_gene_variant | MODIFIER | c.-4973G>A| |
S134 |