Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59510 | A09 | 57589218 | C | T | upstream_gene_variant | MODIFIER | c.-3305C>T| |
S301 S304 |
2 | BAA09g59510 | A09 | 57589792 | T | C | upstream_gene_variant | MODIFIER | c.-2731T>C| |
S94 |
3 | BAA09g59510 | A09 | 57589819 | G | A | upstream_gene_variant | MODIFIER | c.-2704G>A| |
S221 |
4 | BAA09g59510 | A09 | 57589904 | G | A | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S281 |
5 | BAA09g59510 | A09 | 57592696 | C | T | synonymous_variant | LOW | c.174C>T|p.His58His |
S223 |
6 | BAA09g59510 | A09 | 57592700 | C | T | missense_variant | MODERATE | c.178C>T|p.Leu60Phe |
S121 |
7 | BAA09g59510 | A09 | 57592815 | C | T | splice_region_variant&intron_variant | LOW | c.285+8C>T| |
S96 |
8 | BAA09g59510 | A09 | 57593209 | G | A | missense_variant | MODERATE | c.410G>A|p.Arg137Lys |
S238 |
9 | BAA09g59510 | A09 | 57593695 | C | T | splice_region_variant&intron_variant | LOW | c.700-6C>T| |
S211 S227 |
10 | BAA09g59510 | A09 | 57593977 | C | T | missense_variant | MODERATE | c.976C>T|p.Pro326Ser |
S19 |
11 | BAA09g59510 | A09 | 57594051 | G | A | splice_donor_variant&intron_variant | HIGH | c.1049+1G>A| |
S36 |
12 | BAA09g59510 | A09 | 57594644 | C | T | synonymous_variant | LOW | c.1428C>T|p.Phe476Phe |
S159 |
13 | BAA09g59510 | A09 | 57594912 | G | A | missense_variant | MODERATE | c.1696G>A|p.Glu566Lys |
S117 |
14 | BAA09g59510 | A09 | 57595052 | C | T | synonymous_variant | LOW | c.1836C>T|p.His612His |
S75 S81 |
15 | BAA09g59510 | A09 | 57595826 | G | A | synonymous_variant | LOW | c.2610G>A|p.Lys870Lys |
S271 |
16 | BAA09g59510 | A09 | 57596373 | G | A | missense_variant | MODERATE | c.3029G>A|p.Gly1010Glu |
S244 |
17 | BAA09g59510 | A09 | 57597220 | C | T | missense_variant | MODERATE | c.3365C>T|p.Ala1122Val |
S261 |
18 | BAA09g59510 | A09 | 57602599 | G | A | downstream_gene_variant | MODIFIER | c.*4723G>A| |
S298 |