Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00970 | A08 | 722558 | G | A | synonymous_variant | LOW | c.1821C>T|p.Phe607Phe |
S256 |
2 | BAA08g00970 | A08 | 723310 | G | A | synonymous_variant | LOW | c.1530C>T|p.Tyr510Tyr |
S124 |
3 | BAA08g00970 | A08 | 723850 | C | T | missense_variant | MODERATE | c.1145G>A|p.Gly382Glu |
S134 |
4 | BAA08g00970 | A08 | 724710 | G | A | synonymous_variant | LOW | c.843C>T|p.Arg281Arg |
S271 |
5 | BAA08g00970 | A08 | 724711 | C | T | missense_variant | MODERATE | c.842G>A|p.Arg281His |
S172 S217 |
6 | BAA08g00970 | A08 | 724944 | C | T | missense_variant | MODERATE | c.710G>A|p.Gly237Asp |
S216 |
7 | BAA08g00970 | A08 | 725154 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.501-1G>A| |
S261 |
8 | BAA08g00970 | A08 | 725240 | G | A | missense_variant&splice_region_variant | MODERATE | c.500C>T|p.Thr167Ile |
S130 |
9 | BAA08g00970 | A08 | 725267 | C | T | missense_variant | MODERATE | c.473G>A|p.Gly158Glu |
S308 |
10 | BAA08g00970 | A08 | 726076 | G | A | splice_region_variant&synonymous_variant | LOW | c.192C>T|p.His64His |
S192 |
11 | BAA08g00970 | A08 | 726141 | G | A | missense_variant | MODERATE | c.127C>T|p.Pro43Ser |
S81 S85 |
12 | BAA08g00970 | A08 | 726417 | C | T | upstream_gene_variant | MODIFIER | c.-150G>A| |
S95 |
13 | BAA08g00970 | A08 | 726450 | C | T | upstream_gene_variant | MODIFIER | c.-183G>A| |
S191 |
14 | BAA08g00970 | A08 | 728589 | G | A | upstream_gene_variant | MODIFIER | c.-2322C>T| |
S19 |
15 | BAA08g00970 | A08 | 730632 | G | A | upstream_gene_variant | MODIFIER | c.-4365C>T| |
S206 |
16 | BAA08g00970 | A08 | 731053 | C | T | upstream_gene_variant | MODIFIER | c.-4786G>A| |
S142 |