Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19060 | A06 | 9758739 | G | A | missense_variant | MODERATE | c.26G>A|p.Gly9Asp |
S126 |
2 | BAA06g19060 | A06 | 9759435 | G | A | missense_variant | MODERATE | c.556G>A|p.Glu186Lys |
S105 S106 |
3 | BAA06g19060 | A06 | 9760161 | C | T | splice_region_variant&intron_variant | LOW | c.1183-3C>T| |
S247 |
4 | BAA06g19060 | A06 | 9761220 | G | A | missense_variant | MODERATE | c.1870G>A|p.Asp624Asn |
S206 S26 |
5 | BAA06g19060 | A06 | 9763473 | C | T | downstream_gene_variant | MODIFIER | c.*1822C>T| |
S296 |
6 | BAA06g19060 | A06 | 9764743 | C | T | downstream_gene_variant | MODIFIER | c.*3092C>T| |
S293 |
7 | BAA06g19060 | A06 | 9765342 | C | T | downstream_gene_variant | MODIFIER | c.*3691C>T| |
S269 |
8 | BAA06g19060 | A06 | 9765558 | G | A | downstream_gene_variant | MODIFIER | c.*3907G>A| |
S159 S187 S188 S243 S276 |
9 | BAA06g19060 | A06 | 9766141 | C | T | downstream_gene_variant | MODIFIER | c.*4490C>T| |
S36 |
10 | BAA06g19060 | A06 | 9766147 | C | T | downstream_gene_variant | MODIFIER | c.*4496C>T| |
S294 |
11 | BAA06g19060 | A06 | 9766433 | G | A | downstream_gene_variant | MODIFIER | c.*4782G>A| |
S105 S106 |
12 | BAA06g19060 | A06 | 9766610 | G | A | downstream_gene_variant | MODIFIER | c.*4959G>A| |
S136 |