Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g18410 | A05 | 10533471 | C | T | missense_variant | MODERATE | c.2699G>A|p.Ser900Asn |
S177 |
2 | BAA05g18410 | A05 | 10533963 | C | T | synonymous_variant | LOW | c.2367G>A|p.Leu789Leu |
S181 |
3 | BAA05g18410 | A05 | 10535435 | C | T | missense_variant | MODERATE | c.1696G>A|p.Gly566Ser |
S188 |
4 | BAA05g18410 | A05 | 10536130 | C | T | synonymous_variant | LOW | c.1308G>A|p.Gly436Gly |
S261 |
5 | BAA05g18410 | A05 | 10536363 | C | T | synonymous_variant | LOW | c.1200G>A|p.Glu400Glu |
S205 |
6 | BAA05g18410 | A05 | 10537540 | C | T | synonymous_variant | LOW | c.720G>A|p.Glu240Glu |
S135 |
7 | BAA05g18410 | A05 | 10537562 | G | A | missense_variant | MODERATE | c.698C>T|p.Ser233Phe |
S116 |
8 | BAA05g18410 | A05 | 10539177 | C | T | intron_variant | MODIFIER | c.4-127G>A| |
S278 |
9 | BAA05g18410 | A05 | 10539195 | G | A | intron_variant | MODIFIER | c.4-145C>T| |
S158 |
10 | BAA05g18410 | A05 | 10539340 | C | T | intron_variant | MODIFIER | c.3+30G>A| |
S8 |
11 | BAA05g18410 | A05 | 10539641 | G | A | upstream_gene_variant | MODIFIER | c.-269C>T| |
S187 |
12 | BAA05g18410 | A05 | 10540692 | G | A | upstream_gene_variant | MODIFIER | c.-1320C>T| |
S231 |
13 | BAA05g18410 | A05 | 10541550 | G | A | upstream_gene_variant | MODIFIER | c.-2178C>T| |
S129 |
14 | BAA05g18410 | A05 | 10542821 | C | T | upstream_gene_variant | MODIFIER | c.-3449G>A| |
S172 |
15 | BAA05g18410 | A05 | 10543863 | C | T | upstream_gene_variant | MODIFIER | c.-4491G>A| |
S20 |