Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g22990 | A05 | 27617774 | C | T | missense_variant | MODERATE | c.2602G>A|p.Glu868Lys |
S233 |
2 | BAA05g22990 | A05 | 27619115 | C | T | missense_variant | MODERATE | c.1948G>A|p.Gly650Arg |
S242 |
3 | BAA05g22990 | A05 | 27619640 | G | A | synonymous_variant | LOW | c.1614C>T|p.Ile538Ile |
S234 |
4 | BAA05g22990 | A05 | 27619799 | G | A | synonymous_variant | LOW | c.1455C>T|p.Asp485Asp |
S151 S263 |
5 | BAA05g22990 | A05 | 27619958 | C | T | synonymous_variant | LOW | c.1296G>A|p.Val432Val |
S162 |
6 | BAA05g22990 | A05 | 27620025 | G | A | splice_region_variant&intron_variant | LOW | c.1232-3C>T| |
S187 |
7 | BAA05g22990 | A05 | 27621599 | C | T | synonymous_variant | LOW | c.1077G>A|p.Pro359Pro |
S271 S306 |
8 | BAA05g22990 | A05 | 27621654 | G | A | missense_variant | MODERATE | c.1022C>T|p.Pro341Leu |
S282 |
9 | BAA05g22990 | A05 | 27622130 | C | T | intron_variant | MODIFIER | c.826+18G>A| |
S65 |
10 | BAA05g22990 | A05 | 27622634 | C | T | missense_variant | MODERATE | c.340G>A|p.Asp114Asn |
S271 |
11 | BAA05g22990 | A05 | 27622649 | C | T | missense_variant | MODERATE | c.325G>A|p.Asp109Asn |
S247 |
12 | BAA05g22990 | A05 | 27623636 | C | T | upstream_gene_variant | MODIFIER | c.-588G>A| |
S230 |
13 | BAA05g22990 | A05 | 27623677 | G | A | upstream_gene_variant | MODIFIER | c.-629C>T| |
S265 |
14 | BAA05g22990 | A05 | 27624948 | C | T | upstream_gene_variant | MODIFIER | c.-1900G>A| |
S226 |
15 | BAA05g22990 | A05 | 27625045 | G | A | upstream_gene_variant | MODIFIER | c.-1997C>T| |
S219 |
16 | BAA05g22990 | A05 | 27625189 | C | T | upstream_gene_variant | MODIFIER | c.-2141G>A| |
S267 |
17 | BAA05g22990 | A05 | 27625255 | C | T | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S99 |