Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50480 | A09 | 53340705 | G | A | upstream_gene_variant | MODIFIER | c.-1237G>A| |
S216 |
2 | BAA09g50480 | A09 | 53341307 | C | T | upstream_gene_variant | MODIFIER | c.-635C>T| |
S103 |
3 | BAA09g50480 | A09 | 53341759 | G | A | upstream_gene_variant | MODIFIER | c.-183G>A| |
S36 |
4 | BAA09g50480 | A09 | 53342071 | C | T | intron_variant | MODIFIER | c.105+25C>T| |
S163 |
5 | BAA09g50480 | A09 | 53342114 | G | A | intron_variant | MODIFIER | c.106-27G>A| |
S132 S137 S215 S89 |
6 | BAA09g50480 | A09 | 53342315 | G | A | intron_variant | MODIFIER | c.198-12G>A| |
S271 |
7 | BAA09g50480 | A09 | 53342568 | G | A | missense_variant&splice_region_variant | MODERATE | c.370G>A|p.Asp124Asn |
S202 |
8 | BAA09g50480 | A09 | 53344001 | G | A | missense_variant | MODERATE | c.1165G>A|p.Ala389Thr |
S54 |
9 | BAA09g50480 | A09 | 53344279 | C | T | missense_variant | MODERATE | c.1321C>T|p.Leu441Phe |
S205 |
10 | BAA09g50480 | A09 | 53344740 | G | A | missense_variant | MODERATE | c.1403G>A|p.Gly468Glu |
S79 S84 |
11 | BAA09g50480 | A09 | 53345836 | G | A | intron_variant | MODIFIER | c.1931+25G>A| |
S86 |
12 | BAA09g50480 | A09 | 53346339 | C | T | stop_gained | HIGH | c.2197C>T|p.Gln733* |
S100 |
13 | BAA09g50480 | A09 | 53347907 | C | T | missense_variant | MODERATE | c.3056C>T|p.Ser1019Phe |
S237 |