Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g19960 | A03 | 8861357 | C | T | upstream_gene_variant | MODIFIER | c.-3756C>T| |
S251 |
2 | BAA03g19960 | A03 | 8862097 | C | T | upstream_gene_variant | MODIFIER | c.-3016C>T| |
S211 |
3 | BAA03g19960 | A03 | 8862905 | C | T | upstream_gene_variant | MODIFIER | c.-2208C>T| |
S125 |
4 | BAA03g19960 | A03 | 8863532 | G | A | upstream_gene_variant | MODIFIER | c.-1581G>A| |
S111 |
5 | BAA03g19960 | A03 | 8865184 | G | A | synonymous_variant | LOW | c.72G>A|p.Arg24Arg |
S239 |
6 | BAA03g19960 | A03 | 8865192 | G | A | missense_variant | MODERATE | c.80G>A|p.Arg27His |
S225 S73 |
7 | BAA03g19960 | A03 | 8865777 | C | T | splice_region_variant&intron_variant | LOW | c.513+4C>T| |
S171 |
8 | BAA03g19960 | A03 | 8866168 | G | A | intron_variant | MODIFIER | c.514-192G>A| |
S95 |
9 | BAA03g19960 | A03 | 8866737 | C | T | synonymous_variant | LOW | c.708C>T|p.Tyr236Tyr |
S279 |
10 | BAA03g19960 | A03 | 8867008 | G | A | splice_donor_variant&intron_variant | HIGH | c.978+1G>A| |
S13 |
11 | BAA03g19960 | A03 | 8868224 | C | T | missense_variant | MODERATE | c.1895C>T|p.Pro632Leu |
S17 |
12 | BAA03g19960 | A03 | 8869361 | G | A | missense_variant | MODERATE | c.2443G>A|p.Asp815Asn |
S233 S259 |
13 | BAA03g19960 | A03 | 8869964 | C | T | missense_variant | MODERATE | c.2888C>T|p.Ser963Phe |
S191 |
14 | BAA03g19960 | A03 | 8870682 | G | A | missense_variant | MODERATE | c.3370G>A|p.Glu1124Lys |
S290 |
15 | BAA03g19960 | A03 | 8870730 | C | T | missense_variant | MODERATE | c.3418C>T|p.Leu1140Phe |
S34 |
16 | BAA03g19960 | A03 | 8871024 | G | A | missense_variant | MODERATE | c.3643G>A|p.Gly1215Arg |
S109 |
17 | BAA03g19960 | A03 | 8872787 | G | A | downstream_gene_variant | MODIFIER | c.*903G>A| |
S78 |