Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18370 | A09 | 11036152 | G | A | upstream_gene_variant | MODIFIER | c.-4965G>A| |
S244 |
2 | BAA09g18370 | A09 | 11036821 | G | A | upstream_gene_variant | MODIFIER | c.-4296G>A| |
S46 |
3 | BAA09g18370 | A09 | 11037203 | C | T | upstream_gene_variant | MODIFIER | c.-3914C>T| |
S303 |
4 | BAA09g18370 | A09 | 11037630 | C | T | upstream_gene_variant | MODIFIER | c.-3487C>T| |
S2 |
5 | BAA09g18370 | A09 | 11038879 | C | T | upstream_gene_variant | MODIFIER | c.-2238C>T| |
S228 |
6 | BAA09g18370 | A09 | 11040195 | C | T | upstream_gene_variant | MODIFIER | c.-922C>T| |
S306 |
7 | BAA09g18370 | A09 | 11041367 | C | T | intron_variant | MODIFIER | c.212+39C>T| |
S15 S3 |
8 | BAA09g18370 | A09 | 11041569 | C | T | synonymous_variant | LOW | c.372C>T|p.Ile124Ile |
S9 |
9 | BAA09g18370 | A09 | 11042335 | C | T | intron_variant | MODIFIER | c.618-172C>T| |
S132 S215 |
10 | BAA09g18370 | A09 | 11042538 | G | A | missense_variant | MODERATE | c.649G>A|p.Glu217Lys |
S184 |
11 | BAA09g18370 | A09 | 11042632 | G | A | missense_variant&splice_region_variant | MODERATE | c.743G>A|p.Arg248Lys |
S259 |
12 | BAA09g18370 | A09 | 11043847 | C | T | downstream_gene_variant | MODIFIER | c.*635C>T| |
S292 |
13 | BAA09g18370 | A09 | 11045435 | C | G | downstream_gene_variant | MODIFIER | c.*2223C>G| |
S138 |
14 | BAA09g18370 | A09 | 11046356 | G | A | downstream_gene_variant | MODIFIER | c.*3144G>A| |
S12 |
15 | BAA09g18370 | A09 | 11046427 | G | A | downstream_gene_variant | MODIFIER | c.*3215G>A| |
S34 |
16 | BAA09g18370 | A09 | 11048009 | C | T | downstream_gene_variant | MODIFIER | c.*4797C>T| |
S136 |