Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g29690 | A03 | 13896352 | C | T | missense_variant | MODERATE | c.1826G>A|p.Gly609Glu |
S18 |
2 | BAA03g29690 | A03 | 13896427 | C | T | intron_variant | MODIFIER | c.1803+43G>A| |
S294 |
3 | BAA03g29690 | A03 | 13896481 | G | A | missense_variant | MODERATE | c.1792C>T|p.Leu598Phe |
S52 |
4 | BAA03g29690 | A03 | 13897068 | C | T | missense_variant | MODERATE | c.1522G>A|p.Gly508Arg |
S82 S92 |
5 | BAA03g29690 | A03 | 13897097 | C | T | missense_variant | MODERATE | c.1493G>A|p.Arg498Lys |
S99 |
6 | BAA03g29690 | A03 | 13897136 | C | T | missense_variant | MODERATE | c.1454G>A|p.Arg485Lys |
S25 |
7 | BAA03g29690 | A03 | 13897666 | G | A | synonymous_variant | LOW | c.1341C>T|p.Leu447Leu |
S143 |
8 | BAA03g29690 | A03 | 13898087 | C | T | synonymous_variant | LOW | c.1086G>A|p.Glu362Glu |
S87 |
9 | BAA03g29690 | A03 | 13899449 | C | T | missense_variant | MODERATE | c.580G>A|p.Glu194Lys |
S299 |
10 | BAA03g29690 | A03 | 13900414 | G | A | synonymous_variant | LOW | c.229C>T|p.Leu77Leu |
S200 |
11 | BAA03g29690 | A03 | 13900539 | G | A | missense_variant | MODERATE | c.185C>T|p.Ser62Phe |
S57 |
12 | BAA03g29690 | A03 | 13900962 | C | T | splice_region_variant&intron_variant | LOW | c.110+8G>A| |
S113 |
13 | BAA03g29690 | A03 | 13902746 | C | T | upstream_gene_variant | MODIFIER | c.-1667G>A| |
S293 |
14 | BAA03g29690 | A03 | 13903470 | G | A | upstream_gene_variant | MODIFIER | c.-2391C>T| |
S9 |
15 | BAA03g29690 | A03 | 13903944 | G | A | upstream_gene_variant | MODIFIER | c.-2865C>T| |
S172 |
16 | BAA03g29690 | A03 | 13904400 | G | A | upstream_gene_variant | MODIFIER | c.-3321C>T| |
S183 S198 |