Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08050 | A09 | 4495845 | G | A | missense_variant | MODERATE | c.67G>A|p.Glu23Lys |
S180 |
2 | BAA09g08050 | A09 | 4496543 | C | T | missense_variant | MODERATE | c.671C>T|p.Ala224Val |
S126 S127 S131 S190 S255 S287 S57 S58 S60 S61 |
3 | BAA09g08050 | A09 | 4497609 | G | A | missense_variant | MODERATE | c.1465G>A|p.Asp489Asn |
S302 |
4 | BAA09g08050 | A09 | 4498207 | G | A | missense_variant | MODERATE | c.1822G>A|p.Asp608Asn |
S221 |
5 | BAA09g08050 | A09 | 4498419 | G | A | splice_region_variant&intron_variant | LOW | c.2030+4G>A| |
S69 |
6 | BAA09g08050 | A09 | 4498531 | G | A | missense_variant | MODERATE | c.2047G>A|p.Gly683Ser |
S268 |
7 | BAA09g08050 | A09 | 4498561 | G | A | missense_variant | MODERATE | c.2077G>A|p.Asp693Asn |
S131 |
8 | BAA09g08050 | A09 | 4499050 | C | T | missense_variant | MODERATE | c.2486C>T|p.Pro829Leu |
S148 |
9 | BAA09g08050 | A09 | 4499088 | G | A | missense_variant | MODERATE | c.2524G>A|p.Gly842Arg |
S18 |
10 | BAA09g08050 | A09 | 4499837 | C | T | downstream_gene_variant | MODIFIER | c.*546C>T| |
S111 |
11 | BAA09g08050 | A09 | 4500086 | C | T | downstream_gene_variant | MODIFIER | c.*795C>T| |
S13 |
12 | BAA09g08050 | A09 | 4501010 | G | A | downstream_gene_variant | MODIFIER | c.*1719G>A| |
S36 |