Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g64920 | A03 | 38866792 | G | A | downstream_gene_variant | MODIFIER | c.*3696C>T| |
S67 |
2 | BAA03g64920 | A03 | 38868112 | G | A | downstream_gene_variant | MODIFIER | c.*2376C>T| |
S83 S88 |
3 | BAA03g64920 | A03 | 38869087 | G | A | downstream_gene_variant | MODIFIER | c.*1401C>T| |
S245 |
4 | BAA03g64920 | A03 | 38869489 | G | A | downstream_gene_variant | MODIFIER | c.*999C>T| |
S177 |
5 | BAA03g64920 | A03 | 38870439 | C | T | downstream_gene_variant | MODIFIER | c.*49G>A| |
S45 |
6 | BAA03g64920 | A03 | 38870851 | G | A | synonymous_variant | LOW | c.1491C>T|p.Val497Val |
S192 |
7 | BAA03g64920 | A03 | 38871827 | C | T | synonymous_variant | LOW | c.801G>A|p.Arg267Arg |
S161 |
8 | BAA03g64920 | A03 | 38871980 | C | T | missense_variant | MODERATE | c.791G>A|p.Ser264Asn |
S32 |
9 | BAA03g64920 | A03 | 38872588 | G | A | missense_variant | MODERATE | c.430C>T|p.Pro144Ser |
S257 |
10 | BAA03g64920 | A03 | 38872775 | G | A | intron_variant | MODIFIER | c.392-59C>T| |
S152 |
11 | BAA03g64920 | A03 | 38873359 | C | T | missense_variant | MODERATE | c.137G>A|p.Gly46Asp |
S202 |
12 | BAA03g64920 | A03 | 38874448 | C | T | upstream_gene_variant | MODIFIER | c.-553G>A| |
S194 |
13 | BAA03g64920 | A03 | 38874950 | G | A | upstream_gene_variant | MODIFIER | c.-1055C>T| |
S128 |
14 | BAA03g64920 | A03 | 38875161 | C | T | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S14 |
15 | BAA03g64920 | A03 | 38875224 | T | A | upstream_gene_variant | MODIFIER | c.-1329A>T| |
S294 |
16 | BAA03g64920 | A03 | 38875391 | C | T | upstream_gene_variant | MODIFIER | c.-1496G>A| |
S302 |
17 | BAA03g64920 | A03 | 38876843 | C | T | upstream_gene_variant | MODIFIER | c.-2948G>A| |
S200 |