Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05060 | A07 | 4387735 | G | A | upstream_gene_variant | MODIFIER | c.-4601G>A| |
S259 |
2 | BAA07g05060 | A07 | 4388061 | C | T | upstream_gene_variant | MODIFIER | c.-4275C>T| |
S212 |
3 | BAA07g05060 | A07 | 4389462 | C | T | upstream_gene_variant | MODIFIER | c.-2874C>T| |
S205 |
4 | BAA07g05060 | A07 | 4391010 | G | A | upstream_gene_variant | MODIFIER | c.-1326G>A| |
S288 |
5 | BAA07g05060 | A07 | 4391135 | C | T | upstream_gene_variant | MODIFIER | c.-1201C>T| |
S20 |
6 | BAA07g05060 | A07 | 4391357 | C | T | upstream_gene_variant | MODIFIER | c.-979C>T| |
S165 |
7 | BAA07g05060 | A07 | 4391631 | G | A | upstream_gene_variant | MODIFIER | c.-705G>A| |
S206 S26 |
8 | BAA07g05060 | A07 | 4392288 | C | T | upstream_gene_variant | MODIFIER | c.-48C>T| |
S263 |
9 | BAA07g05060 | A07 | 4392560 | G | A | missense_variant&splice_region_variant | MODERATE | c.71G>A|p.Gly24Glu |
S125 |
10 | BAA07g05060 | A07 | 4393284 | C | T | synonymous_variant | LOW | c.795C>T|p.Asp265Asp |
S181 |
11 | BAA07g05060 | A07 | 4393521 | G | A | missense_variant | MODERATE | c.1032G>A|p.Met344Ile |
S233 |
12 | BAA07g05060 | A07 | 4394424 | G | A | synonymous_variant | LOW | c.1587G>A|p.Leu529Leu |
S6 |
13 | BAA07g05060 | A07 | 4395297 | G | A | missense_variant&splice_region_variant | MODERATE | c.2368G>A|p.Val790Ile |
S67 |
14 | BAA07g05060 | A07 | 4395610 | G | A | missense_variant | MODERATE | c.2527G>A|p.Ala843Thr |
S278 |