Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g46790 | A06 | 29643763 | C | T | missense_variant | MODERATE | c.4984G>A|p.Glu1662Lys |
S288 |
2 | BAA06g46790 | A06 | 29643867 | G | A | missense_variant | MODERATE | c.4880C>T|p.Pro1627Leu |
S193 |
3 | BAA06g46790 | A06 | 29644844 | C | T | stop_gained | HIGH | c.4032G>A|p.Trp1344* |
S166 |
4 | BAA06g46790 | A06 | 29645418 | G | A | missense_variant | MODERATE | c.3724C>T|p.Pro1242Ser |
S219 S72 |
5 | BAA06g46790 | A06 | 29645570 | G | A | missense_variant | MODERATE | c.3572C>T|p.Thr1191Ile |
S156 |
6 | BAA06g46790 | A06 | 29645964 | C | T | missense_variant | MODERATE | c.3344G>A|p.Arg1115Lys |
S48 |
7 | BAA06g46790 | A06 | 29646069 | G | A | missense_variant | MODERATE | c.3239C>T|p.Ser1080Phe |
S30 S31 |
8 | BAA06g46790 | A06 | 29646449 | G | A | missense_variant | MODERATE | c.3058C>T|p.Pro1020Ser |
S289 S290 |
9 | BAA06g46790 | A06 | 29646866 | C | T | missense_variant | MODERATE | c.2641G>A|p.Gly881Ser |
S25 |
10 | BAA06g46790 | A06 | 29647221 | G | A | missense_variant | MODERATE | c.2546C>T|p.Ser849Phe |
S160 |
11 | BAA06g46790 | A06 | 29647254 | C | T | missense_variant | MODERATE | c.2513G>A|p.Gly838Asp |
S74 |
12 | BAA06g46790 | A06 | 29647263 | G | A | missense_variant | MODERATE | c.2504C>T|p.Ala835Val |
S40 S49 |
13 | BAA06g46790 | A06 | 29647336 | G | A | missense_variant | MODERATE | c.2431C>T|p.Leu811Phe |
S298 |
14 | BAA06g46790 | A06 | 29647933 | G | A | missense_variant | MODERATE | c.2174C>T|p.Ser725Phe |
S118 |
15 | BAA06g46790 | A06 | 29649478 | C | T | missense_variant | MODERATE | c.1150G>A|p.Glu384Lys |
S259 |
16 | BAA06g46790 | A06 | 29651267 | C | T | upstream_gene_variant | MODIFIER | c.-568G>A| |
S78 |
17 | BAA06g46790 | A06 | 29653703 | G | A | upstream_gene_variant | MODIFIER | c.-3004C>T| |
S90 |
18 | BAA06g46790 | A06 | 29654057 | G | A | upstream_gene_variant | MODIFIER | c.-3358C>T| |
S157 |