Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g32830 | A05 | 34790848 | G | T | missense_variant | MODERATE | c.187G>T|p.Val63Leu |
S299 |
2 | BAA05g32830 | A05 | 34791251 | C | T | missense_variant | MODERATE | c.590C>T|p.Ser197Phe |
S146 |
3 | BAA05g32830 | A05 | 34791920 | G | A | missense_variant | MODERATE | c.1259G>A|p.Arg420Gln |
S163 |
4 | BAA05g32830 | A05 | 34792041 | G | A | synonymous_variant | LOW | c.1380G>A|p.Glu460Glu |
S159 S187 S188 S243 S276 S298 S299 |
5 | BAA05g32830 | A05 | 34792151 | C | T | missense_variant | MODERATE | c.1490C>T|p.Ala497Val |
S236 |
6 | BAA05g32830 | A05 | 34792513 | C | T | missense_variant | MODERATE | c.1852C>T|p.Leu618Phe |
S162 |
7 | BAA05g32830 | A05 | 34792776 | G | A | synonymous_variant | LOW | c.2115G>A|p.Val705Val |
S136 |
8 | BAA05g32830 | A05 | 34792833 | G | A | synonymous_variant | LOW | c.2172G>A|p.Gly724Gly |
S224 |
9 | BAA05g32830 | A05 | 34792941 | C | T | synonymous_variant | LOW | c.2280C>T|p.Asn760Asn |
S242 |
10 | BAA05g32830 | A05 | 34793292 | C | T | synonymous_variant | LOW | c.2631C>T|p.Pro877Pro |
S131 |
11 | BAA05g32830 | A05 | 34793307 | G | A | synonymous_variant | LOW | c.2646G>A|p.Thr882Thr |
S247 |
12 | BAA05g32830 | A05 | 34794149 | C | T | missense_variant | MODERATE | c.3488C>T|p.Ser1163Phe |
S293 |
13 | BAA05g32830 | A05 | 34794236 | G | A | missense_variant | MODERATE | c.3575G>A|p.Arg1192Gln |
S281 |
14 | BAA05g32830 | A05 | 34794460 | C | T | stop_gained | HIGH | c.3799C>T|p.Arg1267* |
S209 |
15 | BAA05g32830 | A05 | 34794661 | G | A | missense_variant | MODERATE | c.4000G>A|p.Gly1334Arg |
S75 S81 |
16 | BAA05g32830 | A05 | 34794799 | G | A | missense_variant | MODERATE | c.4138G>A|p.Glu1380Lys |
S267 |
17 | BAA05g32830 | A05 | 34795637 | C | T | downstream_gene_variant | MODIFIER | c.*773C>T| |
S43 |