Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g40220 | A05 | 38991908 | C | T | stop_gained | HIGH | c.55C>T|p.Gln19* |
S13 |
2 | BAA05g40220 | A05 | 38992121 | G | A | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S61 |
3 | BAA05g40220 | A05 | 38992178 | C | T | missense_variant | MODERATE | c.325C>T|p.Pro109Ser |
S65 |
4 | BAA05g40220 | A05 | 38992245 | G | A | missense_variant | MODERATE | c.392G>A|p.Gly131Glu |
S171 |
5 | BAA05g40220 | A05 | 38992383 | C | T | missense_variant | MODERATE | c.530C>T|p.Ser177Phe |
S268 |
6 | BAA05g40220 | A05 | 38992442 | G | A | missense_variant | MODERATE | c.589G>A|p.Asp197Asn |
S308 |
7 | BAA05g40220 | A05 | 38992749 | G | A | missense_variant | MODERATE | c.896G>A|p.Arg299Gln |
S161 |
8 | BAA05g40220 | A05 | 38992955 | C | T | missense_variant | MODERATE | c.1102C>T|p.Pro368Ser |
S296 |
9 | BAA05g40220 | A05 | 38993894 | G | A | synonymous_variant | LOW | c.1620G>A|p.Glu540Glu |
S283 |
10 | BAA05g40220 | A05 | 38994248 | G | A | synonymous_variant | LOW | c.1890G>A|p.Lys630Lys |
S62 |
11 | BAA05g40220 | A05 | 38994273 | C | T | missense_variant | MODERATE | c.1915C>T|p.Leu639Phe |
S32 |
12 | BAA05g40220 | A05 | 38994425 | G | A | synonymous_variant | LOW | c.2067G>A|p.Ser689Ser |
S236 |
13 | BAA05g40220 | A05 | 38994778 | G | A | missense_variant | MODERATE | c.2420G>A|p.Arg807Lys |
S232 |
14 | BAA05g40220 | A05 | 38998443 | G | A | downstream_gene_variant | MODIFIER | c.*3625G>A| |
S188 |