Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17390 | A06 | 8757193 | C | T | missense_variant | MODERATE | c.3067G>A|p.Asp1023Asn |
S80 |
2 | BAA06g17390 | A06 | 8759545 | G | A | synonymous_variant | LOW | c.1731C>T|p.Cys577Cys |
S130 |
3 | BAA06g17390 | A06 | 8759609 | C | T | missense_variant | MODERATE | c.1667G>A|p.Cys556Tyr |
S257 |
4 | BAA06g17390 | A06 | 8760606 | G | A | missense_variant | MODERATE | c.1268C>T|p.Ala423Val |
S224 |
5 | BAA06g17390 | A06 | 8760954 | C | T | stop_gained&splice_region_variant | HIGH | c.1094G>A|p.Trp365* |
S67 |
6 | BAA06g17390 | A06 | 8761247 | C | T | intron_variant | MODIFIER | c.1021-36G>A| |
S111 |
7 | BAA06g17390 | A06 | 8762752 | C | T | intron_variant | MODIFIER | c.370+32G>A| |
S156 |
8 | BAA06g17390 | A06 | 8763496 | G | A | upstream_gene_variant | MODIFIER | c.-343C>T| |
S302 |
9 | BAA06g17390 | A06 | 8763940 | G | A | upstream_gene_variant | MODIFIER | c.-787C>T| |
S135 S203 S68 |
10 | BAA06g17390 | A06 | 8764654 | C | T | upstream_gene_variant | MODIFIER | c.-1501G>A| |
S189 |
11 | BAA06g17390 | A06 | 8764945 | C | T | upstream_gene_variant | MODIFIER | c.-1792G>A| |
S293 |
12 | BAA06g17390 | A06 | 8765029 | G | A | upstream_gene_variant | MODIFIER | c.-1876C>T| |
S206 S26 |
13 | BAA06g17390 | A06 | 8767391 | G | A | upstream_gene_variant | MODIFIER | c.-4238C>T| |
S153 |
14 | BAA06g17390 | A06 | 8767752 | C | T | upstream_gene_variant | MODIFIER | c.-4599G>A| |
S2 |
15 | BAA06g17390 | A06 | 8767958 | C | T | upstream_gene_variant | MODIFIER | c.-4805G>A| |
S103 |