Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g63680 | A03 | 32651310 | G | A | missense_variant | MODERATE | c.1556C>T|p.Pro519Leu |
S229 |
2 | BAA03g63680 | A03 | 32651378 | G | A | synonymous_variant | LOW | c.1488C>T|p.Ser496Ser |
S233 |
3 | BAA03g63680 | A03 | 32651665 | C | T | missense_variant | MODERATE | c.1201G>A|p.Asp401Asn |
S252 |
4 | BAA03g63680 | A03 | 32651777 | C | T | synonymous_variant | LOW | c.1089G>A|p.Arg363Arg |
S81 S85 |
5 | BAA03g63680 | A03 | 32651899 | C | T | missense_variant | MODERATE | c.967G>A|p.Gly323Arg |
S157 S201 |
6 | BAA03g63680 | A03 | 32651972 | C | T | synonymous_variant | LOW | c.894G>A|p.Lys298Lys |
S187 |
7 | BAA03g63680 | A03 | 32652164 | G | A | synonymous_variant | LOW | c.702C>T|p.Asn234Asn |
S296 |
8 | BAA03g63680 | A03 | 32652359 | G | A | synonymous_variant | LOW | c.507C>T|p.Leu169Leu |
S280 |
9 | BAA03g63680 | A03 | 32652499 | C | T | splice_region_variant&intron_variant | LOW | c.373-6G>A| |
S274 |
10 | BAA03g63680 | A03 | 32652611 | G | A | synonymous_variant | LOW | c.339C>T|p.Phe113Phe |
S278 |
11 | BAA03g63680 | A03 | 32654130 | G | A | upstream_gene_variant | MODIFIER | c.-1181C>T| |
S136 |
12 | BAA03g63680 | A03 | 32655248 | G | A | upstream_gene_variant | MODIFIER | c.-2299C>T| |
S276 |
13 | BAA03g63680 | A03 | 32656507 | G | A | upstream_gene_variant | MODIFIER | c.-3558C>T| |
S136 |
14 | BAA03g63680 | A03 | 32656635 | G | A | upstream_gene_variant | MODIFIER | c.-3686C>T| |
S123 |
15 | BAA03g63680 | A03 | 32657170 | G | A | upstream_gene_variant | MODIFIER | c.-4221C>T| |
S135 |
16 | BAA03g63680 | A03 | 32657206 | C | T | upstream_gene_variant | MODIFIER | c.-4257G>A| |
S32 |
17 | BAA03g63680 | A03 | 32657251 | C | T | upstream_gene_variant | MODIFIER | c.-4302G>A| |
S231 |
18 | BAA03g63680 | A03 | 32657767 | G | A | upstream_gene_variant | MODIFIER | c.-4818C>T| |
S236 |
19 | BAA03g63680 | A03 | 32657855 | G | A | upstream_gene_variant | MODIFIER | c.-4906C>T| |
S237 |