Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17440 | A09 | 10411034 | G | A | intron_variant | MODIFIER | c.622-361C>T| |
S113 |
2 | BAA09g17440 | A09 | 10411161 | C | T | intron_variant | MODIFIER | c.622-488G>A| |
S284 |
3 | BAA09g17440 | A09 | 10412395 | C | T | missense_variant | MODERATE | c.530G>A|p.Cys177Tyr |
S71 |
4 | BAA09g17440 | A09 | 10412507 | C | T | intron_variant | MODIFIER | c.480+25G>A| |
S153 |
5 | BAA09g17440 | A09 | 10412580 | C | G | synonymous_variant | LOW | c.432G>C|p.Pro144Pro |
S294 |
6 | BAA09g17440 | A09 | 10413178 | C | T | upstream_gene_variant | MODIFIER | c.-167G>A| |
S286 |
7 | BAA09g17440 | A09 | 10413254 | C | T | upstream_gene_variant | MODIFIER | c.-243G>A| |
S96 |
8 | BAA09g17440 | A09 | 10413620 | G | A | upstream_gene_variant | MODIFIER | c.-609C>T| |
S298 |
9 | BAA09g17440 | A09 | 10413802 | G | A | upstream_gene_variant | MODIFIER | c.-791C>T| |
S128 |
10 | BAA09g17440 | A09 | 10414384 | G | A | upstream_gene_variant | MODIFIER | c.-1373C>T| |
S162 |
11 | BAA09g17440 | A09 | 10414599 | C | T | upstream_gene_variant | MODIFIER | c.-1588G>A| |
S293 |
12 | BAA09g17440 | A09 | 10414812 | G | A | upstream_gene_variant | MODIFIER | c.-1801C>T| |
S233 |
13 | BAA09g17440 | A09 | 10414835 | G | A | upstream_gene_variant | MODIFIER | c.-1824C>T| |
S83 S88 S92 |
14 | BAA09g17440 | A09 | 10415828 | T | C | upstream_gene_variant | MODIFIER | c.-2817A>G| |
S42 |
15 | BAA09g17440 | A09 | 10415997 | C | T | upstream_gene_variant | MODIFIER | c.-2986G>A| |
S41 |
16 | BAA09g17440 | A09 | 10416607 | G | A | upstream_gene_variant | MODIFIER | c.-3596C>T| |
S280 |
17 | BAA09g17440 | A09 | 10416936 | C | T | upstream_gene_variant | MODIFIER | c.-3925G>A| |
S283 |
18 | BAA09g17440 | A09 | 10417407 | C | T | upstream_gene_variant | MODIFIER | c.-4396G>A| |
S211 S227 |