Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05870 | A09 | 3317679 | C | T | missense_variant | MODERATE | c.3398G>A|p.Arg1133Gln |
S98 |
2 | BAA09g05870 | A09 | 3318402 | G | A | missense_variant | MODERATE | c.2675C>T|p.Ala892Val |
S45 |
3 | BAA09g05870 | A09 | 3318625 | G | A | intron_variant | MODIFIER | c.2650+67C>T| |
S202 |
4 | BAA09g05870 | A09 | 3318700 | G | A | missense_variant | MODERATE | c.2642C>T|p.Ser881Phe |
S259 |
5 | BAA09g05870 | A09 | 3318710 | C | T | missense_variant | MODERATE | c.2632G>A|p.Ala878Thr |
S10 |
6 | BAA09g05870 | A09 | 3320607 | G | A | synonymous_variant | LOW | c.1563C>T|p.Tyr521Tyr |
S142 |
7 | BAA09g05870 | A09 | 3321405 | C | T | missense_variant | MODERATE | c.1076G>A|p.Arg359Lys |
S87 |
8 | BAA09g05870 | A09 | 3321676 | G | A | missense_variant | MODERATE | c.881C>T|p.Pro294Leu |
S11 |
9 | BAA09g05870 | A09 | 3322767 | G | A | synonymous_variant | LOW | c.171C>T|p.Ser57Ser |
S20 |
10 | BAA09g05870 | A09 | 3323391 | C | T | upstream_gene_variant | MODIFIER | c.-454G>A| |
S284 |
11 | BAA09g05870 | A09 | 3323597 | G | A | upstream_gene_variant | MODIFIER | c.-660C>T| |
S225 |
12 | BAA09g05870 | A09 | 3324030 | C | T | upstream_gene_variant | MODIFIER | c.-1093G>A| |
S19 |
13 | BAA09g05870 | A09 | 3324057 | T | A | upstream_gene_variant | MODIFIER | c.-1120A>T| |
S149 |
14 | BAA09g05870 | A09 | 3326034 | G | A | upstream_gene_variant | MODIFIER | c.-3097C>T| |
S182 |
15 | BAA09g05870 | A09 | 3327840 | G | A | upstream_gene_variant | MODIFIER | c.-4903C>T| |
S116 |