Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g43640 | A06 | 28058110 | G | A | missense_variant | MODERATE | c.2275C>T|p.Pro759Ser |
S20 |
2 | BAA06g43640 | A06 | 28058209 | G | A | stop_gained | HIGH | c.2176C>T|p.Gln726* |
S293 |
3 | BAA06g43640 | A06 | 28059003 | C | T | missense_variant | MODERATE | c.1481G>A|p.Arg494Gln |
S192 |
4 | BAA06g43640 | A06 | 28059676 | G | A | synonymous_variant | LOW | c.1152C>T|p.Ala384Ala |
S204 |
5 | BAA06g43640 | A06 | 28059731 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Phe |
S87 |
6 | BAA06g43640 | A06 | 28060542 | G | A | synonymous_variant | LOW | c.531C>T|p.Leu177Leu |
S118 S132 |
7 | BAA06g43640 | A06 | 28060634 | C | T | missense_variant | MODERATE | c.439G>A|p.Gly147Arg |
S167 |
8 | BAA06g43640 | A06 | 28061447 | C | T | upstream_gene_variant | MODIFIER | c.-55G>A| |
S288 |
9 | BAA06g43640 | A06 | 28062732 | G | A | upstream_gene_variant | MODIFIER | c.-1340C>T| |
S293 |
10 | BAA06g43640 | A06 | 28062760 | C | T | upstream_gene_variant | MODIFIER | c.-1368G>A| |
S246 |
11 | BAA06g43640 | A06 | 28063833 | G | A | upstream_gene_variant | MODIFIER | c.-2441C>T| |
S289 S290 |
12 | BAA06g43640 | A06 | 28065733 | A | C | upstream_gene_variant | MODIFIER | c.-4341T>G| |
S201 |
13 | BAA06g43640 | A06 | 28066154 | G | A | upstream_gene_variant | MODIFIER | c.-4762C>T| |
S162 |