Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g35260 | A05 | 35992708 | G | A | missense_variant | MODERATE | c.121G>A|p.Ala41Thr |
S104 S52 |
2 | BAA05g35260 | A05 | 35995550 | C | T | intron_variant | MODIFIER | c.1397+93C>T| |
S216 |
3 | BAA05g35260 | A05 | 35995969 | G | A | intron_variant | MODIFIER | c.1477-33G>A| |
S107 |
4 | BAA05g35260 | A05 | 35997156 | G | A | intron_variant | MODIFIER | c.1947+196G>A| |
S305 |
5 | BAA05g35260 | A05 | 35997802 | C | T | intron_variant | MODIFIER | c.2115-38C>T| |
S4 |
6 | BAA05g35260 | A05 | 35998689 | C | T | splice_region_variant&intron_variant | LOW | c.2457-3C>T| |
S206 S26 |
7 | BAA05g35260 | A05 | 35998855 | G | A | missense_variant | MODERATE | c.2620G>A|p.Ala874Thr |
S272 |
8 | BAA05g35260 | A05 | 36000386 | C | T | missense_variant | MODERATE | c.3098C>T|p.Ser1033Phe |
S37 |
9 | BAA05g35260 | A05 | 36000591 | C | T | missense_variant | MODERATE | c.3175C>T|p.Pro1059Ser |
S4 |
10 | BAA05g35260 | A05 | 36000667 | C | T | intron_variant | MODIFIER | c.3219+32C>T| |
S264 |
11 | BAA05g35260 | A05 | 36000895 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.3307-1G>A| |
S51 |
12 | BAA05g35260 | A05 | 36001540 | C | T | downstream_gene_variant | MODIFIER | c.*603C>T| |
S242 |