Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g27730 | A08 | 19449471 | G | A | missense_variant | MODERATE | c.218G>A|p.Gly73Asp |
S185 |
2 | BAA08g27730 | A08 | 19449507 | C | T | missense_variant | MODERATE | c.254C>T|p.Pro85Leu |
S228 |
3 | BAA08g27730 | A08 | 19449611 | G | A | missense_variant | MODERATE | c.358G>A|p.Gly120Arg |
S272 |
4 | BAA08g27730 | A08 | 19450740 | G | A | missense_variant | MODERATE | c.1096G>A|p.Ala366Thr |
S246 |
5 | BAA08g27730 | A08 | 19451204 | C | T | missense_variant | MODERATE | c.1469C>T|p.Ser490Phe |
S136 |
6 | BAA08g27730 | A08 | 19451431 | C | T | missense_variant | MODERATE | c.1520C>T|p.Pro507Leu |
S149 |
7 | BAA08g27730 | A08 | 19453686 | C | T | downstream_gene_variant | MODIFIER | c.*1088C>T| |
S18 |
8 | BAA08g27730 | A08 | 19453826 | C | T | downstream_gene_variant | MODIFIER | c.*1228C>T| |
S192 |
9 | BAA08g27730 | A08 | 19454106 | G | A | downstream_gene_variant | MODIFIER | c.*1508G>A| |
S56 |
10 | BAA08g27730 | A08 | 19454176 | C | T | downstream_gene_variant | MODIFIER | c.*1578C>T| |
S270 |
11 | BAA08g27730 | A08 | 19454272 | G | A | downstream_gene_variant | MODIFIER | c.*1674G>A| |
S229 |
12 | BAA08g27730 | A08 | 19454287 | G | A | downstream_gene_variant | MODIFIER | c.*1689G>A| |
S245 |
13 | BAA08g27730 | A08 | 19454690 | G | A | downstream_gene_variant | MODIFIER | c.*2092G>A| |
S264 |
14 | BAA08g27730 | A08 | 19456434 | C | T | downstream_gene_variant | MODIFIER | c.*3836C>T| |
S51 |
15 | BAA08g27730 | A08 | 19456834 | C | T | downstream_gene_variant | MODIFIER | c.*4236C>T| |
S242 |
16 | BAA08g27730 | A08 | 19457406 | C | T | downstream_gene_variant | MODIFIER | c.*4808C>T| |
S135 |