Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04740 | A02 | 2052980 | G | A | missense_variant | MODERATE | c.1651C>T|p.Pro551Ser |
S166 |
2 | BAA02g04740 | A02 | 2053719 | C | T | missense_variant | MODERATE | c.1298G>A|p.Arg433His |
S288 |
3 | BAA02g04740 | A02 | 2053996 | C | T | missense_variant | MODERATE | c.1155G>A|p.Met385Ile |
S79 S84 |
4 | BAA02g04740 | A02 | 2054899 | G | A | missense_variant | MODERATE | c.790C>T|p.Leu264Phe |
S134 |
5 | BAA02g04740 | A02 | 2055420 | G | A | synonymous_variant | LOW | c.426C>T|p.Asn142Asn |
S105 S106 |
6 | BAA02g04740 | A02 | 2055446 | C | T | missense_variant | MODERATE | c.400G>A|p.Val134Ile |
S278 |
7 | BAA02g04740 | A02 | 2056366 | C | T | missense_variant | MODERATE | c.83G>A|p.Ser28Asn |
S87 |
8 | BAA02g04740 | A02 | 2056386 | C | T | synonymous_variant | LOW | c.63G>A|p.Glu21Glu |
S179 |
9 | BAA02g04740 | A02 | 2056851 | C | T | upstream_gene_variant | MODIFIER | c.-403G>A| |
S121 |
10 | BAA02g04740 | A02 | 2057003 | G | A | upstream_gene_variant | MODIFIER | c.-555C>T| |
S276 |
11 | BAA02g04740 | A02 | 2057251 | G | A | upstream_gene_variant | MODIFIER | c.-803C>T| |
S96 |
12 | BAA02g04740 | A02 | 2057660 | C | T | upstream_gene_variant | MODIFIER | c.-1212G>A| |
S278 |
13 | BAA02g04740 | A02 | 2057695 | C | T | upstream_gene_variant | MODIFIER | c.-1247G>A| |
S250 |
14 | BAA02g04740 | A02 | 2057722 | G | A | upstream_gene_variant | MODIFIER | c.-1274C>T| |
S259 |
15 | BAA02g04740 | A02 | 2060092 | G | A | upstream_gene_variant | MODIFIER | c.-3644C>T| |
S153 S213 |
16 | BAA02g04740 | A02 | 2060346 | G | A | upstream_gene_variant | MODIFIER | c.-3898C>T| |
S146 |