Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18530 | A10 | 17313277 | G | A | splice_region_variant&intron_variant | LOW | c.1787-3C>T| |
S162 |
2 | BAA10g18530 | A10 | 17314284 | G | A | synonymous_variant | LOW | c.1110C>T|p.His370His |
S172 S217 |
3 | BAA10g18530 | A10 | 17314356 | G | A | synonymous_variant | LOW | c.1038C>T|p.Phe346Phe |
S138 |
4 | BAA10g18530 | A10 | 17314499 | G | A | missense_variant | MODERATE | c.895C>T|p.Leu299Phe |
S69 |
5 | BAA10g18530 | A10 | 17314513 | C | T | missense_variant | MODERATE | c.881G>A|p.Ser294Asn |
S236 |
6 | BAA10g18530 | A10 | 17314616 | G | A | synonymous_variant | LOW | c.778C>T|p.Leu260Leu |
S240 |
7 | BAA10g18530 | A10 | 17314921 | G | A | missense_variant | MODERATE | c.473C>T|p.Ser158Phe |
S138 |
8 | BAA10g18530 | A10 | 17315552 | G | A | upstream_gene_variant | MODIFIER | c.-159C>T| |
S4 |
9 | BAA10g18530 | A10 | 17316098 | C | T | upstream_gene_variant | MODIFIER | c.-705G>A| |
S201 |
10 | BAA10g18530 | A10 | 17318250 | G | A | upstream_gene_variant | MODIFIER | c.-2857C>T| |
S129 |
11 | BAA10g18530 | A10 | 17318407 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S139 |
12 | BAA10g18530 | A10 | 17318419 | G | A | upstream_gene_variant | MODIFIER | c.-3026C>T| |
S184 |
13 | BAA10g18530 | A10 | 17318569 | G | A | upstream_gene_variant | MODIFIER | c.-3176C>T| |
S159 |
14 | BAA10g18530 | A10 | 17318761 | G | A | upstream_gene_variant | MODIFIER | c.-3368C>T| |
S303 |
15 | BAA10g18530 | A10 | 17319530 | G | A | upstream_gene_variant | MODIFIER | c.-4137C>T| |
S38 |
16 | BAA10g18530 | A10 | 17319886 | G | A | upstream_gene_variant | MODIFIER | c.-4493C>T| |
S295 |