Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22780 | A01 | 11521443 | C | T | missense_variant | MODERATE | c.59C>T|p.Thr20Met |
S46 |
2 | BAA01g22780 | A01 | 11521746 | G | A | missense_variant | MODERATE | c.362G>A|p.Ser121Asn |
S195 |
3 | BAA01g22780 | A01 | 11521992 | G | A | missense_variant | MODERATE | c.608G>A|p.Arg203His |
S180 |
4 | BAA01g22780 | A01 | 11522180 | C | T | missense_variant | MODERATE | c.796C>T|p.Pro266Ser |
S289 S290 |
5 | BAA01g22780 | A01 | 11522538 | C | T | missense_variant | MODERATE | c.1154C>T|p.Thr385Ile |
S260 |
6 | BAA01g22780 | A01 | 11524121 | C | T | missense_variant | MODERATE | c.1834C>T|p.Pro612Ser |
S198 |
7 | BAA01g22780 | A01 | 11526498 | G | A | intron_variant | MODIFIER | c.2269-597G>A| |
S262 |
8 | BAA01g22780 | A01 | 11527382 | C | T | synonymous_variant | LOW | c.2556C>T|p.Pro852Pro |
S67 |
9 | BAA01g22780 | A01 | 11527428 | G | A | missense_variant | MODERATE | c.2602G>A|p.Glu868Lys |
S287 |
10 | BAA01g22780 | A01 | 11528597 | C | T | downstream_gene_variant | MODIFIER | c.*406C>T| |
S264 |
11 | BAA01g22780 | A01 | 11528810 | C | T | downstream_gene_variant | MODIFIER | c.*619C>T| |
S242 |
12 | BAA01g22780 | A01 | 11529008 | G | A | downstream_gene_variant | MODIFIER | c.*817G>A| |
S276 |
13 | BAA01g22780 | A01 | 11529139 | G | A | downstream_gene_variant | MODIFIER | c.*948G>A| |
S172 S217 |
14 | BAA01g22780 | A01 | 11529473 | G | A | downstream_gene_variant | MODIFIER | c.*1282G>A| |
S301 S304 |
15 | BAA01g22780 | A01 | 11529517 | T | A | downstream_gene_variant | MODIFIER | c.*1326T>A| |
S62 |
16 | BAA01g22780 | A01 | 11529781 | G | A | downstream_gene_variant | MODIFIER | c.*1590G>A| |
S298 |