Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00670 | Scaffold13 | 7785662 | G | A | downstream_gene_variant | MODIFIER | c.*4550C>T| |
S68 |
2 | BAS13g00670 | Scaffold13 | 7786321 | A | T | downstream_gene_variant | MODIFIER | c.*3891T>A| |
S87 |
3 | BAS13g00670 | Scaffold13 | 7786438 | G | A | downstream_gene_variant | MODIFIER | c.*3774C>T| |
S294 |
4 | BAS13g00670 | Scaffold13 | 7787299 | G | A | downstream_gene_variant | MODIFIER | c.*2913C>T| |
S243 S299 |
5 | BAS13g00670 | Scaffold13 | 7787867 | C | T | downstream_gene_variant | MODIFIER | c.*2345G>A| |
S25 |
6 | BAS13g00670 | Scaffold13 | 7787941 | C | T | downstream_gene_variant | MODIFIER | c.*2271G>A| |
S32 |
7 | BAS13g00670 | Scaffold13 | 7790779 | T | G | missense_variant | MODERATE | c.1331A>C|p.Lys444Thr |
S201 |
8 | BAS13g00670 | Scaffold13 | 7790971 | G | A | missense_variant | MODERATE | c.1139C>T|p.Pro380Leu |
S82 S92 |
9 | BAS13g00670 | Scaffold13 | 7791008 | C | T | missense_variant | MODERATE | c.1102G>A|p.Glu368Lys |
S197 |
10 | BAS13g00670 | Scaffold13 | 7791041 | C | T | missense_variant | MODERATE | c.1069G>A|p.Val357Ile |
S71 |
11 | BAS13g00670 | Scaffold13 | 7791149 | C | T | missense_variant | MODERATE | c.961G>A|p.Glu321Lys |
S144 |
12 | BAS13g00670 | Scaffold13 | 7791642 | C | T | stop_gained | HIGH | c.642G>A|p.Trp214* |
S240 |
13 | BAS13g00670 | Scaffold13 | 7791651 | C | T | synonymous_variant | LOW | c.633G>A|p.Thr211Thr |
S95 |
14 | BAS13g00670 | Scaffold13 | 7793679 | C | T | upstream_gene_variant | MODIFIER | c.-812G>A| |
S37 |
15 | BAS13g00670 | Scaffold13 | 7793759 | C | T | upstream_gene_variant | MODIFIER | c.-892G>A| |
S153 |
16 | BAS13g00670 | Scaffold13 | 7793928 | A | C | upstream_gene_variant | MODIFIER | c.-1061T>G| |
S261 |
17 | BAS13g00670 | Scaffold13 | 7793941 | C | T | upstream_gene_variant | MODIFIER | c.-1074G>A| |
S95 |
18 | BAS13g00670 | Scaffold13 | 7794279 | C | T | upstream_gene_variant | MODIFIER | c.-1412G>A| |
S133 |
19 | BAS13g00670 | Scaffold13 | 7794568 | C | T | upstream_gene_variant | MODIFIER | c.-1701G>A| |
S13 |
20 | BAS13g00670 | Scaffold13 | 7794588 | G | A | upstream_gene_variant | MODIFIER | c.-1721C>T| |
S181 |
21 | BAS13g00670 | Scaffold13 | 7794691 | C | T | upstream_gene_variant | MODIFIER | c.-1824G>A| |
S2 |
22 | BAS13g00670 | Scaffold13 | 7795271 | C | T | upstream_gene_variant | MODIFIER | c.-2404G>A| |
S48 |
23 | BAS13g00670 | Scaffold13 | 7796059 | G | A | upstream_gene_variant | MODIFIER | c.-3192C>T| |
S164 |
24 | BAS13g00670 | Scaffold13 | 7796084 | C | T | upstream_gene_variant | MODIFIER | c.-3217G>A| |
S230 |
25 | BAS13g00670 | Scaffold13 | 7796364 | C | T | upstream_gene_variant | MODIFIER | c.-3497G>A| |
S37 |