Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42980 | A05 | 40517398 | G | A | downstream_gene_variant | MODIFIER | c.*2146C>T| |
S65 |
2 | BAA05g42980 | A05 | 40517648 | G | A | downstream_gene_variant | MODIFIER | c.*1896C>T| |
S298 |
3 | BAA05g42980 | A05 | 40517658 | G | A | downstream_gene_variant | MODIFIER | c.*1886C>T| |
S140 |
4 | BAA05g42980 | A05 | 40518465 | G | A | downstream_gene_variant | MODIFIER | c.*1079C>T| |
S11 |
5 | BAA05g42980 | A05 | 40518490 | G | A | downstream_gene_variant | MODIFIER | c.*1054C>T| |
S177 |
6 | BAA05g42980 | A05 | 40520450 | G | A | missense_variant | MODERATE | c.608C>T|p.Ala203Val |
S79 S91 |
7 | BAA05g42980 | A05 | 40520567 | G | A | splice_region_variant&intron_variant | LOW | c.494-3C>T| |
S294 |
8 | BAA05g42980 | A05 | 40520698 | G | A | missense_variant | MODERATE | c.458C>T|p.Ser153Phe |
S110 |
9 | BAA05g42980 | A05 | 40520844 | G | A | synonymous_variant | LOW | c.312C>T|p.Tyr104Tyr |
S129 |
10 | BAA05g42980 | A05 | 40524717 | C | T | upstream_gene_variant | MODIFIER | c.-3123G>A| |
S224 |
11 | BAA05g42980 | A05 | 40525906 | C | T | upstream_gene_variant | MODIFIER | c.-4312G>A| |
S245 |