Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19650 | A06 | 10187376 | G | A | upstream_gene_variant | MODIFIER | c.-539G>A| |
S13 |
2 | BAA06g19650 | A06 | 10187449 | C | T | upstream_gene_variant | MODIFIER | c.-466C>T| |
S211 S227 |
3 | BAA06g19650 | A06 | 10187498 | G | A | upstream_gene_variant | MODIFIER | c.-417G>A| |
S95 |
4 | BAA06g19650 | A06 | 10188214 | G | A | synonymous_variant | LOW | c.300G>A|p.Glu100Glu |
S161 |
5 | BAA06g19650 | A06 | 10188827 | G | A | missense_variant | MODERATE | c.616G>A|p.Asp206Asn |
S146 |
6 | BAA06g19650 | A06 | 10189145 | G | A | missense_variant | MODERATE | c.850G>A|p.Gly284Arg |
S231 |
7 | BAA06g19650 | A06 | 10189455 | C | T | missense_variant | MODERATE | c.1160C>T|p.Thr387Met |
S286 |
8 | BAA06g19650 | A06 | 10190341 | C | T | synonymous_variant | LOW | c.2046C>T|p.Tyr682Tyr |
S221 |
9 | BAA06g19650 | A06 | 10190846 | G | A | missense_variant | MODERATE | c.2551G>A|p.Glu851Lys |
S217 |
10 | BAA06g19650 | A06 | 10191098 | C | T | synonymous_variant | LOW | c.2803C>T|p.Leu935Leu |
S263 |
11 | BAA06g19650 | A06 | 10192129 | C | T | synonymous_variant | LOW | c.3834C>T|p.Leu1278Leu |
S10 |
12 | BAA06g19650 | A06 | 10192242 | G | A | missense_variant | MODERATE | c.3947G>A|p.Ser1316Asn |
S51 |
13 | BAA06g19650 | A06 | 10192724 | G | A | missense_variant | MODERATE | c.4429G>A|p.Glu1477Lys |
S45 |