Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g36070 | A06 | 23990225 | G | A | downstream_gene_variant | MODIFIER | c.*2079C>T| |
S202 |
2 | BAA06g36070 | A06 | 23992509 | C | T | missense_variant | MODERATE | c.1778G>A|p.Gly593Asp |
S172 S217 |
3 | BAA06g36070 | A06 | 23992708 | C | T | synonymous_variant | LOW | c.1677G>A|p.Glu559Glu |
S5 |
4 | BAA06g36070 | A06 | 23992716 | C | T | missense_variant | MODERATE | c.1669G>A|p.Ala557Thr |
S167 S5 |
5 | BAA06g36070 | A06 | 23993095 | G | A | splice_region_variant&intron_variant | LOW | c.1533+4C>T| |
S224 |
6 | BAA06g36070 | A06 | 23993378 | G | A | synonymous_variant | LOW | c.1356C>T|p.Cys452Cys |
S17 |
7 | BAA06g36070 | A06 | 23993904 | G | A | missense_variant | MODERATE | c.1013C>T|p.Ser338Phe |
S239 |
8 | BAA06g36070 | A06 | 23994029 | C | T | stop_gained | HIGH | c.888G>A|p.Trp296* |
S247 |
9 | BAA06g36070 | A06 | 23994863 | C | T | missense_variant | MODERATE | c.218G>A|p.Gly73Asp |
S161 |
10 | BAA06g36070 | A06 | 23995113 | G | A | upstream_gene_variant | MODIFIER | c.-33C>T| |
S261 |
11 | BAA06g36070 | A06 | 23995887 | C | T | upstream_gene_variant | MODIFIER | c.-807G>A| |
S84 S93 |
12 | BAA06g36070 | A06 | 23997504 | G | A | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S66 |
13 | BAA06g36070 | A06 | 23997936 | G | A | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S275 |
14 | BAA06g36070 | A06 | 23999521 | C | T | upstream_gene_variant | MODIFIER | c.-4441G>A| |
S277 |