Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g23110 | A04 | 25244858 | G | A | synonymous_variant | LOW | c.2992C>T|p.Leu998Leu |
S293 |
2 | BAA04g23110 | A04 | 25245350 | C | T | synonymous_variant | LOW | c.2667G>A|p.Glu889Glu |
S32 |
3 | BAA04g23110 | A04 | 25246621 | G | A | synonymous_variant | LOW | c.2085C>T|p.Phe695Phe |
S35 |
4 | BAA04g23110 | A04 | 25246680 | C | T | missense_variant | MODERATE | c.2026G>A|p.Asp676Asn |
S78 |
5 | BAA04g23110 | A04 | 25247106 | C | T | synonymous_variant | LOW | c.1893G>A|p.Gln631Gln |
S42 |
6 | BAA04g23110 | A04 | 25247199 | G | A | synonymous_variant | LOW | c.1800C>T|p.Ala600Ala |
S136 |
7 | BAA04g23110 | A04 | 25247738 | G | A | missense_variant | MODERATE | c.1576C>T|p.Arg526Cys |
S79 S91 |
8 | BAA04g23110 | A04 | 25248605 | G | A | missense_variant | MODERATE | c.1093C>T|p.Leu365Phe |
S297 |
9 | BAA04g23110 | A04 | 25248628 | C | T | missense_variant | MODERATE | c.1070G>A|p.Cys357Tyr |
S204 |
10 | BAA04g23110 | A04 | 25249344 | C | T | missense_variant | MODERATE | c.787G>A|p.Val263Met |
S163 |
11 | BAA04g23110 | A04 | 25250581 | C | T | synonymous_variant | LOW | c.441G>A|p.Val147Val |
S180 |
12 | BAA04g23110 | A04 | 25251044 | G | A | missense_variant | MODERATE | c.304C>T|p.Pro102Ser |
S303 |
13 | BAA04g23110 | A04 | 25251340 | G | A | splice_region_variant&intron_variant | LOW | c.94-3C>T| |
S38 |
14 | BAA04g23110 | A04 | 25253870 | A | T | upstream_gene_variant | MODIFIER | c.-2308T>A| |
S198 |
15 | BAA04g23110 | A04 | 25254230 | C | T | upstream_gene_variant | MODIFIER | c.-2668G>A| |
S189 |
16 | BAA04g23110 | A04 | 25255140 | C | T | upstream_gene_variant | MODIFIER | c.-3578G>A| |
S182 |