Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g18590 | A04 | 22353613 | G | A | upstream_gene_variant | MODIFIER | c.-4848G>A| |
S150 |
2 | BAA04g18590 | A04 | 22354205 | G | A | upstream_gene_variant | MODIFIER | c.-4256G>A| |
S144 |
3 | BAA04g18590 | A04 | 22354938 | G | A | upstream_gene_variant | MODIFIER | c.-3523G>A| |
S264 |
4 | BAA04g18590 | A04 | 22356320 | C | T | upstream_gene_variant | MODIFIER | c.-2141C>T| |
S135 |
5 | BAA04g18590 | A04 | 22357512 | G | A | upstream_gene_variant | MODIFIER | c.-949G>A| |
S202 |
6 | BAA04g18590 | A04 | 22358145 | C | T | upstream_gene_variant | MODIFIER | c.-316C>T| |
S110 |
7 | BAA04g18590 | A04 | 22359498 | G | A | synonymous_variant | LOW | c.1038G>A|p.Lys346Lys |
S125 S302 |
8 | BAA04g18590 | A04 | 22359689 | G | A | missense_variant | MODERATE | c.1229G>A|p.Gly410Glu |
S218 |
9 | BAA04g18590 | A04 | 22360610 | G | A | missense_variant | MODERATE | c.1552G>A|p.Ala518Thr |
S125 |
10 | BAA04g18590 | A04 | 22360632 | C | T | missense_variant | MODERATE | c.1574C>T|p.Ala525Val |
S88 |
11 | BAA04g18590 | A04 | 22361127 | C | T | splice_region_variant&intron_variant | LOW | c.1983+7C>T| |
S207 |
12 | BAA04g18590 | A04 | 22361641 | G | A | missense_variant | MODERATE | c.2437G>A|p.Asp813Asn |
S206 S26 |