Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g34320 | A01 | 22992639 | C | T | splice_region_variant&intron_variant | LOW | c.3078+5G>A| |
S78 S83 |
2 | BAA01g34320 | A01 | 22993484 | C | T | synonymous_variant | LOW | c.2586G>A|p.Gln862Gln |
S51 |
3 | BAA01g34320 | A01 | 22993984 | C | T | synonymous_variant | LOW | c.2322G>A|p.Lys774Lys |
S206 |
4 | BAA01g34320 | A01 | 22994404 | C | T | missense_variant | MODERATE | c.2050G>A|p.Asp684Asn |
S4 |
5 | BAA01g34320 | A01 | 22994513 | C | T | splice_region_variant&synonymous_variant | LOW | c.1941G>A|p.Glu647Glu |
S224 |
6 | BAA01g34320 | A01 | 22995069 | C | T | missense_variant | MODERATE | c.1688G>A|p.Gly563Glu |
S179 S90 |
7 | BAA01g34320 | A01 | 22996587 | G | A | synonymous_variant | LOW | c.867C>T|p.Ile289Ile |
S225 S73 |
8 | BAA01g34320 | A01 | 22996951 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.691-1G>A| |
S155 S211 |
9 | BAA01g34320 | A01 | 22997339 | C | T | missense_variant | MODERATE | c.484G>A|p.Glu162Lys |
S132 S137 |
10 | BAA01g34320 | A01 | 23001358 | G | A | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S172 S217 S58 |
11 | BAA01g34320 | A01 | 23001471 | G | A | upstream_gene_variant | MODIFIER | c.-3311C>T| |
S259 |
12 | BAA01g34320 | A01 | 23002348 | C | T | upstream_gene_variant | MODIFIER | c.-4188G>A| |
S183 S198 |
13 | BAA01g34320 | A01 | 23002634 | G | A | upstream_gene_variant | MODIFIER | c.-4474C>T| |
S71 |
14 | BAA01g34320 | A01 | 23002895 | C | T | upstream_gene_variant | MODIFIER | c.-4735G>A| |
S180 |
15 | BAA01g34320 | A01 | 23003085 | G | A | upstream_gene_variant | MODIFIER | c.-4925C>T| |
S36 |