Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20290 | A10 | 18303842 | G | A | missense_variant | MODERATE | c.1786C>T|p.Pro596Ser |
S109 |
2 | BAA10g20290 | A10 | 18303909 | G | A | synonymous_variant | LOW | c.1719C>T|p.Asn573Asn |
S218 |
3 | BAA10g20290 | A10 | 18303986 | C | T | missense_variant | MODERATE | c.1642G>A|p.Glu548Lys |
S110 |
4 | BAA10g20290 | A10 | 18304360 | C | T | missense_variant | MODERATE | c.1441G>A|p.Val481Ile |
S119 |
5 | BAA10g20290 | A10 | 18304913 | G | A | missense_variant | MODERATE | c.1141C>T|p.Pro381Ser |
S273 |
6 | BAA10g20290 | A10 | 18305697 | G | A | synonymous_variant | LOW | c.772C>T|p.Leu258Leu |
S164 |
7 | BAA10g20290 | A10 | 18307673 | C | T | synonymous_variant | LOW | c.120G>A|p.Ala40Ala |
S266 |
8 | BAA10g20290 | A10 | 18308353 | G | A | upstream_gene_variant | MODIFIER | c.-561C>T| |
S286 |
9 | BAA10g20290 | A10 | 18308392 | G | A | upstream_gene_variant | MODIFIER | c.-600C>T| |
S80 |
10 | BAA10g20290 | A10 | 18308678 | C | T | upstream_gene_variant | MODIFIER | c.-886G>A| |
S60 |
11 | BAA10g20290 | A10 | 18309238 | C | T | upstream_gene_variant | MODIFIER | c.-1446G>A| |
S77 |
12 | BAA10g20290 | A10 | 18310788 | G | A | upstream_gene_variant | MODIFIER | c.-2996C>T| |
S33 |
13 | BAA10g20290 | A10 | 18311448 | G | A | upstream_gene_variant | MODIFIER | c.-3656C>T| |
S239 |
14 | BAA10g20290 | A10 | 18311513 | G | T | upstream_gene_variant | MODIFIER | c.-3721C>A| |
S187 |
15 | BAA10g20290 | A10 | 18311567 | G | A | upstream_gene_variant | MODIFIER | c.-3775C>T| |
S284 |
16 | BAA10g20290 | A10 | 18311826 | G | A | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S160 |
17 | BAA10g20290 | A10 | 18311931 | G | A | upstream_gene_variant | MODIFIER | c.-4139C>T| |
S13 S140 S278 S279 S64 |