Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g28050 | A03 | 12975651 | G | A | upstream_gene_variant | MODIFIER | c.-161G>A| |
S15 S156 S3 |
2 | BAA03g28050 | A03 | 12976036 | C | T | missense_variant | MODERATE | c.146C>T|p.Thr49Ile |
S96 |
3 | BAA03g28050 | A03 | 12976350 | G | A | missense_variant | MODERATE | c.379G>A|p.Asp127Asn |
S259 |
4 | BAA03g28050 | A03 | 12976476 | T | C | missense_variant | MODERATE | c.437T>C|p.Leu146Pro |
S286 |
5 | BAA03g28050 | A03 | 12976681 | C | T | synonymous_variant | LOW | c.642C>T|p.Tyr214Tyr |
S256 |
6 | BAA03g28050 | A03 | 12976684 | G | A | synonymous_variant | LOW | c.645G>A|p.Lys215Lys |
S259 |
7 | BAA03g28050 | A03 | 12978158 | C | T | missense_variant | MODERATE | c.1285C>T|p.Pro429Ser |
S275 |
8 | BAA03g28050 | A03 | 12978355 | G | A | missense_variant | MODERATE | c.1408G>A|p.Asp470Asn |
S289 S290 |
9 | BAA03g28050 | A03 | 12978901 | C | T | missense_variant&splice_region_variant | MODERATE | c.1618C>T|p.His540Tyr |
S156 |
10 | BAA03g28050 | A03 | 12979304 | G | A | stop_gained | HIGH | c.1869G>A|p.Trp623* |
S107 |
11 | BAA03g28050 | A03 | 12979608 | G | A | missense_variant | MODERATE | c.1996G>A|p.Asp666Asn |
S291 |