Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g19900 | A04 | 23204252 | C | T | upstream_gene_variant | MODIFIER | c.-1711C>T| |
S107 |
2 | BAA04g19900 | A04 | 23206266 | G | A | missense_variant&splice_region_variant | MODERATE | c.228G>A|p.Met76Ile |
S190 |
3 | BAA04g19900 | A04 | 23207454 | G | A | splice_donor_variant&intron_variant | HIGH | c.647+1G>A| |
S239 |
4 | BAA04g19900 | A04 | 23207546 | C | T | synonymous_variant | LOW | c.666C>T|p.Tyr222Tyr |
S81 S85 |
5 | BAA04g19900 | A04 | 23207831 | C | T | synonymous_variant | LOW | c.951C>T|p.Asn317Asn |
S216 |
6 | BAA04g19900 | A04 | 23207866 | C | T | missense_variant | MODERATE | c.986C>T|p.Ser329Phe |
S279 |
7 | BAA04g19900 | A04 | 23208132 | C | T | missense_variant | MODERATE | c.1252C>T|p.Leu418Phe |
S10 |
8 | BAA04g19900 | A04 | 23211092 | C | T | downstream_gene_variant | MODIFIER | c.*2619C>T| |
S295 |
9 | BAA04g19900 | A04 | 23211728 | G | A | downstream_gene_variant | MODIFIER | c.*3255G>A| |
S234 |
10 | BAA04g19900 | A04 | 23212308 | C | T | downstream_gene_variant | MODIFIER | c.*3835C>T| |
S138 |
11 | BAA04g19900 | A04 | 23212554 | C | T | downstream_gene_variant | MODIFIER | c.*4081C>T| |
S292 |