Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g07120 | A01 | 3154353 | C | T | upstream_gene_variant | MODIFIER | c.-2964C>T| |
S61 |
2 | BAA01g07120 | A01 | 3155088 | C | G | upstream_gene_variant | MODIFIER | c.-2229C>G| |
S276 |
3 | BAA01g07120 | A01 | 3155647 | G | A | upstream_gene_variant | MODIFIER | c.-1670G>A| |
S195 |
4 | BAA01g07120 | A01 | 3157322 | G | A | synonymous_variant | LOW | c.6G>A|p.Lys2Lys |
S146 |
5 | BAA01g07120 | A01 | 3157634 | G | A | intron_variant | MODIFIER | c.127+191G>A| |
S121 |
6 | BAA01g07120 | A01 | 3157639 | G | A | intron_variant | MODIFIER | c.127+196G>A| |
S57 |
7 | BAA01g07120 | A01 | 3159460 | T | G | missense_variant | MODERATE | c.1206T>G|p.Phe402Leu |
S156 S157 S17 S243 S270 |
8 | BAA01g07120 | A01 | 3160493 | T | G | missense_variant | MODERATE | c.1661T>G|p.Leu554Arg |
S115 S129 S132 S185 S193 S222 S223 S237 S238 S239 S246 S251 S252 S259 S261 S276 S293 |
9 | BAA01g07120 | A01 | 3160730 | C | T | missense_variant | MODERATE | c.1898C>T|p.Ala633Val |
S42 |
10 | BAA01g07120 | A01 | 3161530 | G | A | synonymous_variant | LOW | c.2157G>A|p.Arg719Arg |
S103 |
11 | BAA01g07120 | A01 | 3161857 | G | A | synonymous_variant | LOW | c.2484G>A|p.Pro828Pro |
S23 |
12 | BAA01g07120 | A01 | 3163344 | G | A | downstream_gene_variant | MODIFIER | c.*1145G>A| |
S190 |
13 | BAA01g07120 | A01 | 3166641 | G | A | downstream_gene_variant | MODIFIER | c.*4442G>A| |
S162 |