Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19350 | A09 | 11761193 | G | A | missense_variant | MODERATE | c.1399G>A|p.Asp467Asn |
S86 |
2 | BAA09g19350 | A09 | 11762215 | C | T | missense_variant | MODERATE | c.1646C>T|p.Ser549Phe |
S116 |
3 | BAA09g19350 | A09 | 11762477 | G | A | synonymous_variant | LOW | c.1794G>A|p.Arg598Arg |
S191 |
4 | BAA09g19350 | A09 | 11764047 | C | T | intron_variant | MODIFIER | c.2172+68C>T| |
S54 |
5 | BAA09g19350 | A09 | 11764339 | C | T | splice_region_variant&intron_variant | LOW | c.2173-8C>T| |
S2 |
6 | BAA09g19350 | A09 | 11764815 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.2239-1G>A| |
S126 |
7 | BAA09g19350 | A09 | 11764921 | G | A | intron_variant | MODIFIER | c.2324+20G>A| |
S149 |
8 | BAA09g19350 | A09 | 11765788 | G | A | synonymous_variant | LOW | c.2661G>A|p.Arg887Arg |
S166 |
9 | BAA09g19350 | A09 | 11766603 | C | T | intron_variant | MODIFIER | c.2911-144C>T| |
S242 |
10 | BAA09g19350 | A09 | 11767888 | G | A | missense_variant | MODERATE | c.3328G>A|p.Glu1110Lys |
S38 |
11 | BAA09g19350 | A09 | 11769566 | G | A | missense_variant | MODERATE | c.3787G>A|p.Glu1263Lys |
S73 S91 |
12 | BAA09g19350 | A09 | 11769583 | G | A | stop_gained | HIGH | c.3804G>A|p.Trp1268* |
S75 S81 |
13 | BAA09g19350 | A09 | 11769835 | G | A | missense_variant | MODERATE | c.3989G>A|p.Arg1330Lys |
S204 |
14 | BAA09g19350 | A09 | 11770390 | C | T | missense_variant | MODERATE | c.4217C>T|p.Thr1406Ile |
S139 |
15 | BAA09g19350 | A09 | 11774000 | C | T | downstream_gene_variant | MODIFIER | c.*3357C>T| |
S8 |