Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g31560 | A01 | 20616499 | G | A | downstream_gene_variant | MODIFIER | c.*4147C>T| |
S274 |
2 | BAA01g31560 | A01 | 20617304 | G | A | downstream_gene_variant | MODIFIER | c.*3342C>T| |
S68 |
3 | BAA01g31560 | A01 | 20618189 | G | A | downstream_gene_variant | MODIFIER | c.*2457C>T| |
S232 |
4 | BAA01g31560 | A01 | 20620806 | C | T | missense_variant | MODERATE | c.1022G>A|p.Cys341Tyr |
S81 S85 |
5 | BAA01g31560 | A01 | 20621138 | C | T | missense_variant | MODERATE | c.781G>A|p.Ala261Thr |
S162 |
6 | BAA01g31560 | A01 | 20621313 | G | A | synonymous_variant | LOW | c.606C>T|p.Asp202Asp |
S217 S248 |
7 | BAA01g31560 | A01 | 20621794 | C | T | missense_variant | MODERATE | c.284G>A|p.Gly95Glu |
S150 |
8 | BAA01g31560 | A01 | 20622015 | C | T | splice_region_variant&intron_variant | LOW | c.145+3G>A| |
S171 |
9 | BAA01g31560 | A01 | 20622071 | C | T | missense_variant | MODERATE | c.92G>A|p.Arg31Lys |
S210 |
10 | BAA01g31560 | A01 | 20622295 | C | T | upstream_gene_variant | MODIFIER | c.-133G>A| |
S286 |
11 | BAA01g31560 | A01 | 20622398 | C | T | upstream_gene_variant | MODIFIER | c.-236G>A| |
S192 |
12 | BAA01g31560 | A01 | 20622700 | C | T | upstream_gene_variant | MODIFIER | c.-538G>A| |
S237 |
13 | BAA01g31560 | A01 | 20622910 | C | T | upstream_gene_variant | MODIFIER | c.-748G>A| |
S249 |
14 | BAA01g31560 | A01 | 20624391 | G | A | upstream_gene_variant | MODIFIER | c.-2229C>T| |
S287 |
15 | BAA01g31560 | A01 | 20627032 | G | A | upstream_gene_variant | MODIFIER | c.-4870C>T| |
S165 S32 |