Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05990 | A08 | 4686947 | G | A | downstream_gene_variant | MODIFIER | c.*2299C>T| |
S92 |
2 | BAA08g05990 | A08 | 4687503 | G | A | downstream_gene_variant | MODIFIER | c.*1743C>T| |
S197 |
3 | BAA08g05990 | A08 | 4689280 | C | T | missense_variant | MODERATE | c.1172G>A|p.Gly391Glu |
S294 |
4 | BAA08g05990 | A08 | 4689285 | G | A | synonymous_variant | LOW | c.1167C>T|p.Ser389Ser |
S182 |
5 | BAA08g05990 | A08 | 4689320 | C | T | missense_variant | MODERATE | c.1132G>A|p.Asp378Asn |
S255 |
6 | BAA08g05990 | A08 | 4690093 | G | A | missense_variant | MODERATE | c.473C>T|p.Pro158Leu |
S185 |
7 | BAA08g05990 | A08 | 4690453 | C | T | missense_variant | MODERATE | c.113G>A|p.Arg38Lys |
S83 S88 |
8 | BAA08g05990 | A08 | 4690528 | G | A | intron_variant | MODIFIER | c.52-14C>T| |
S200 |
9 | BAA08g05990 | A08 | 4690616 | C | T | intron_variant | MODIFIER | c.52-102G>A| |
S225 |
10 | BAA08g05990 | A08 | 4690799 | G | A | upstream_gene_variant | MODIFIER | c.-30C>T| |
S200 |
11 | BAA08g05990 | A08 | 4691074 | G | A | upstream_gene_variant | MODIFIER | c.-305C>T| |
S103 |
12 | BAA08g05990 | A08 | 4692035 | C | T | upstream_gene_variant | MODIFIER | c.-1266G>A| |
S265 |
13 | BAA08g05990 | A08 | 4692668 | G | A | upstream_gene_variant | MODIFIER | c.-1899C>T| |
S170 |
14 | BAA08g05990 | A08 | 4693201 | C | T | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S173 |
15 | BAA08g05990 | A08 | 4693616 | G | A | upstream_gene_variant | MODIFIER | c.-2847C>T| |
S221 |
16 | BAA08g05990 | A08 | 4693669 | G | A | upstream_gene_variant | MODIFIER | c.-2900C>T| |
S278 |
17 | BAA08g05990 | A08 | 4694292 | G | A | upstream_gene_variant | MODIFIER | c.-3523C>T| |
S103 |
18 | BAA08g05990 | A08 | 4694611 | G | A | upstream_gene_variant | MODIFIER | c.-3842C>T| |
S301 S304 |
19 | BAA08g05990 | A08 | 4694799 | C | T | upstream_gene_variant | MODIFIER | c.-4030G>A| |
S244 |