Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g23910 | A08 | 17586409 | G | A | synonymous_variant | LOW | c.3429C>T|p.Leu1143Leu |
S35 |
2 | BAA08g23910 | A08 | 17586412 | G | A | synonymous_variant | LOW | c.3426C>T|p.Leu1142Leu |
S291 |
3 | BAA08g23910 | A08 | 17587847 | C | T | missense_variant | MODERATE | c.3140G>A|p.Gly1047Glu |
S178 |
4 | BAA08g23910 | A08 | 17587860 | C | T | missense_variant | MODERATE | c.3127G>A|p.Glu1043Lys |
S113 |
5 | BAA08g23910 | A08 | 17587938 | C | T | missense_variant | MODERATE | c.3049G>A|p.Ala1017Thr |
S274 |
6 | BAA08g23910 | A08 | 17589064 | G | A | synonymous_variant | LOW | c.2607C>T|p.His869His |
S172 S217 |
7 | BAA08g23910 | A08 | 17589486 | C | T | missense_variant | MODERATE | c.2185G>A|p.Asp729Asn |
S148 S210 S30 S31 |
8 | BAA08g23910 | A08 | 17589598 | G | A | synonymous_variant | LOW | c.2073C>T|p.Leu691Leu |
S12 |
9 | BAA08g23910 | A08 | 17590435 | C | T | missense_variant | MODERATE | c.1414G>A|p.Glu472Lys |
S94 |
10 | BAA08g23910 | A08 | 17591776 | C | T | missense_variant | MODERATE | c.73G>A|p.Ala25Thr |
S63 |
11 | BAA08g23910 | A08 | 17591818 | G | A | missense_variant | MODERATE | c.31C>T|p.Leu11Phe |
S302 |
12 | BAA08g23910 | A08 | 17591956 | C | T | upstream_gene_variant | MODIFIER | c.-108G>A| |
S184 |
13 | BAA08g23910 | A08 | 17591982 | G | A | upstream_gene_variant | MODIFIER | c.-134C>T| |
S160 |
14 | BAA08g23910 | A08 | 17593382 | G | A | upstream_gene_variant | MODIFIER | c.-1534C>T| |
S279 |
15 | BAA08g23910 | A08 | 17593762 | G | A | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S58 |
16 | BAA08g23910 | A08 | 17594706 | G | T | upstream_gene_variant | MODIFIER | c.-2858C>A| |
S298 |
17 | BAA08g23910 | A08 | 17594862 | C | T | upstream_gene_variant | MODIFIER | c.-3014G>A| |
S81 S85 |
18 | BAA08g23910 | A08 | 17595192 | T | A | upstream_gene_variant | MODIFIER | c.-3344A>T| |
S180 |
19 | BAA08g23910 | A08 | 17596516 | G | A | upstream_gene_variant | MODIFIER | c.-4668C>T| |
S140 |
20 | BAA08g23910 | A08 | 17596754 | C | T | upstream_gene_variant | MODIFIER | c.-4906G>A| |
S69 |