Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g44890 | A06 | 28686201 | G | A | upstream_gene_variant | MODIFIER | c.-202G>A| |
S121 S48 |
2 | BAA06g44890 | A06 | 28686208 | G | A | upstream_gene_variant | MODIFIER | c.-195G>A| |
S264 |
3 | BAA06g44890 | A06 | 28686712 | C | T | stop_gained | HIGH | c.310C>T|p.Gln104* |
S108 |
4 | BAA06g44890 | A06 | 28686750 | C | T | synonymous_variant | LOW | c.348C>T|p.His116His |
S165 |
5 | BAA06g44890 | A06 | 28686804 | C | T | synonymous_variant | LOW | c.402C>T|p.Ile134Ile |
S260 |
6 | BAA06g44890 | A06 | 28690459 | C | T | intron_variant | MODIFIER | c.495-467C>T| |
S287 |
7 | BAA06g44890 | A06 | 28691141 | G | A | missense_variant | MODERATE | c.710G>A|p.Gly237Glu |
S30 S31 |
8 | BAA06g44890 | A06 | 28691409 | G | A | synonymous_variant | LOW | c.978G>A|p.Lys326Lys |
S171 |
9 | BAA06g44890 | A06 | 28691846 | G | A | missense_variant | MODERATE | c.1415G>A|p.Arg472Lys |
S239 |
10 | BAA06g44890 | A06 | 28691881 | G | A | missense_variant | MODERATE | c.1450G>A|p.Gly484Arg |
S36 |
11 | BAA06g44890 | A06 | 28692183 | C | T | intron_variant | MODIFIER | c.1628+124C>T| |
S223 |
12 | BAA06g44890 | A06 | 28692550 | C | T | intron_variant | MODIFIER | c.1628+491C>T| |
S174 S27 |
13 | BAA06g44890 | A06 | 28692787 | G | A | intron_variant | MODIFIER | c.1628+728G>A| |
S183 S198 |
14 | BAA06g44890 | A06 | 28695634 | G | A | missense_variant | MODERATE | c.1870G>A|p.Glu624Lys |
S138 |
15 | BAA06g44890 | A06 | 28697085 | G | A | downstream_gene_variant | MODIFIER | c.*338G>A| |
S55 |
16 | BAA06g44890 | A06 | 28697315 | G | A | downstream_gene_variant | MODIFIER | c.*568G>A| |
S54 |