Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02440 | A04 | 1441847 | A | T | upstream_gene_variant | MODIFIER | c.-4056A>T| |
S150 |
2 | BAA04g02440 | A04 | 1444175 | C | T | upstream_gene_variant | MODIFIER | c.-1728C>T| |
S231 |
3 | BAA04g02440 | A04 | 1444456 | C | T | upstream_gene_variant | MODIFIER | c.-1447C>T| |
S140 |
4 | BAA04g02440 | A04 | 1444627 | G | A | upstream_gene_variant | MODIFIER | c.-1276G>A| |
S4 |
5 | BAA04g02440 | A04 | 1444698 | G | A | upstream_gene_variant | MODIFIER | c.-1205G>A| |
S262 |
6 | BAA04g02440 | A04 | 1444784 | G | A | upstream_gene_variant | MODIFIER | c.-1119G>A| |
S47 |
7 | BAA04g02440 | A04 | 1444920 | G | A | upstream_gene_variant | MODIFIER | c.-983G>A| |
S108 |
8 | BAA04g02440 | A04 | 1445947 | C | T | synonymous_variant | LOW | c.45C>T|p.Ile15Ile |
S297 |
9 | BAA04g02440 | A04 | 1446388 | G | A | synonymous_variant | LOW | c.486G>A|p.Gln162Gln |
S263 |
10 | BAA04g02440 | A04 | 1446484 | G | A | synonymous_variant | LOW | c.582G>A|p.Lys194Lys |
S161 |
11 | BAA04g02440 | A04 | 1446537 | C | G | missense_variant | MODERATE | c.635C>G|p.Thr212Arg |
S192 |