Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g03540 | A06 | 1986985 | C | T | missense_variant | MODERATE | c.2789G>A|p.Arg930Lys |
S111 |
2 | BAA06g03540 | A06 | 1987401 | C | T | missense_variant | MODERATE | c.2533G>A|p.Asp845Asn |
S66 |
3 | BAA06g03540 | A06 | 1987490 | G | A | missense_variant | MODERATE | c.2444C>T|p.Thr815Ile |
S246 |
4 | BAA06g03540 | A06 | 1987524 | C | T | missense_variant | MODERATE | c.2410G>A|p.Ala804Thr |
S223 |
5 | BAA06g03540 | A06 | 1987632 | G | A | stop_gained | HIGH | c.2302C>T|p.Gln768* |
S58 |
6 | BAA06g03540 | A06 | 1988042 | G | A | synonymous_variant | LOW | c.1980C>T|p.Cys660Cys |
S161 |
7 | BAA06g03540 | A06 | 1989173 | C | T | missense_variant | MODERATE | c.1085G>A|p.Gly362Asp |
S76 |
8 | BAA06g03540 | A06 | 1990396 | G | A | missense_variant | MODERATE | c.445C>T|p.His149Tyr |
S246 |
9 | BAA06g03540 | A06 | 1990408 | G | A | missense_variant | MODERATE | c.433C>T|p.Pro145Ser |
S169 |
10 | BAA06g03540 | A06 | 1990585 | G | A | missense_variant | MODERATE | c.256C>T|p.Pro86Ser |
S202 |
11 | BAA06g03540 | A06 | 1990917 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S92 |
12 | BAA06g03540 | A06 | 1993136 | C | T | upstream_gene_variant | MODIFIER | c.-2216G>A| |
S16 |
13 | BAA06g03540 | A06 | 1993491 | C | T | upstream_gene_variant | MODIFIER | c.-2571G>A| |
S296 |
14 | BAA06g03540 | A06 | 1993557 | G | T | upstream_gene_variant | MODIFIER | c.-2637C>A| |
S30 |
15 | BAA06g03540 | A06 | 1994107 | C | T | upstream_gene_variant | MODIFIER | c.-3187G>A| |
S134 |
16 | BAA06g03540 | A06 | 1995315 | G | A | upstream_gene_variant | MODIFIER | c.-4395C>T| |
S208 S219 |
17 | BAA06g03540 | A06 | 1995561 | C | T | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S245 |