Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g09780 | A04 | 15970295 | G | A | missense_variant | MODERATE | c.512G>A|p.Arg171His |
S261 |
2 | BAA04g09780 | A04 | 15970479 | T | G | synonymous_variant | LOW | c.696T>G|p.Thr232Thr |
S111 |
3 | BAA04g09780 | A04 | 15970644 | C | T | synonymous_variant | LOW | c.861C>T|p.Asn287Asn |
S200 |
4 | BAA04g09780 | A04 | 15970714 | G | A | missense_variant | MODERATE | c.931G>A|p.Glu311Lys |
S126 |
5 | BAA04g09780 | A04 | 15970743 | C | T | synonymous_variant | LOW | c.960C>T|p.Asp320Asp |
S179 |
6 | BAA04g09780 | A04 | 15971045 | G | A | missense_variant | MODERATE | c.1262G>A|p.Arg421Lys |
S284 |
7 | BAA04g09780 | A04 | 15971809 | C | T | missense_variant | MODERATE | c.1624C>T|p.Leu542Phe |
S134 |
8 | BAA04g09780 | A04 | 15972148 | G | A | missense_variant | MODERATE | c.1963G>A|p.Glu655Lys |
S158 |
9 | BAA04g09780 | A04 | 15972194 | C | T | missense_variant | MODERATE | c.2009C>T|p.Pro670Leu |
S15 S3 |
10 | BAA04g09780 | A04 | 15972206 | C | T | missense_variant | MODERATE | c.2021C>T|p.Ala674Val |
S295 |
11 | BAA04g09780 | A04 | 15972410 | G | A | missense_variant | MODERATE | c.2225G>A|p.Arg742His |
S217 S248 |
12 | BAA04g09780 | A04 | 15973426 | G | A | missense_variant&splice_region_variant | MODERATE | c.2375G>A|p.Gly792Glu |
S135 S152 S273 S68 |
13 | BAA04g09780 | A04 | 15973939 | C | T | missense_variant | MODERATE | c.2786C>T|p.Ala929Val |
S202 |
14 | BAA04g09780 | A04 | 15974125 | G | A | downstream_gene_variant | MODIFIER | c.*113G>A| |
S216 |
15 | BAA04g09780 | A04 | 15974386 | G | A | downstream_gene_variant | MODIFIER | c.*374G>A| |
S62 |