Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g56560 | A03 | 27996966 | C | T | missense_variant | MODERATE | c.577G>A|p.Val193Ile |
S2 |
2 | BAA03g56560 | A03 | 27997644 | C | T | intron_variant | MODIFIER | c.478-579G>A| |
S273 |
3 | BAA03g56560 | A03 | 27997690 | G | A | intron_variant | MODIFIER | c.478-625C>T| |
S170 |
4 | BAA03g56560 | A03 | 27997768 | C | T | intron_variant | MODIFIER | c.478-703G>A| |
S207 |
5 | BAA03g56560 | A03 | 27998785 | G | A | intron_variant | MODIFIER | c.477+1141C>T| |
S1 S90 |
6 | BAA03g56560 | A03 | 27999567 | G | A | intron_variant | MODIFIER | c.477+359C>T| |
S295 |
7 | BAA03g56560 | A03 | 28000072 | C | T | missense_variant | MODERATE | c.331G>A|p.Asp111Asn |
S140 |
8 | BAA03g56560 | A03 | 28000684 | G | A | intron_variant | MODIFIER | c.212-493C>T| |
S48 |
9 | BAA03g56560 | A03 | 28002371 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S218 |
10 | BAA03g56560 | A03 | 28002952 | G | A | upstream_gene_variant | MODIFIER | c.-642C>T| |
S237 |
11 | BAA03g56560 | A03 | 28003502 | C | T | upstream_gene_variant | MODIFIER | c.-1192G>A| |
S292 |
12 | BAA03g56560 | A03 | 28007249 | G | A | upstream_gene_variant | MODIFIER | c.-4939C>T| |
S69 |