Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05870 | A10 | 3000573 | G | A | downstream_gene_variant | MODIFIER | c.*3659C>T| |
S236 |
2 | BAA10g05870 | A10 | 3000750 | C | T | downstream_gene_variant | MODIFIER | c.*3482G>A| |
S142 |
3 | BAA10g05870 | A10 | 3000920 | G | A | downstream_gene_variant | MODIFIER | c.*3312C>T| |
S283 |
4 | BAA10g05870 | A10 | 3001027 | G | A | downstream_gene_variant | MODIFIER | c.*3205C>T| |
S234 |
5 | BAA10g05870 | A10 | 3001236 | G | A | downstream_gene_variant | MODIFIER | c.*2996C>T| |
S5 |
6 | BAA10g05870 | A10 | 3001263 | G | A | downstream_gene_variant | MODIFIER | c.*2969C>T| |
S292 |
7 | BAA10g05870 | A10 | 3001505 | G | A | downstream_gene_variant | MODIFIER | c.*2727C>T| |
S151 S263 |
8 | BAA10g05870 | A10 | 3001637 | G | A | downstream_gene_variant | MODIFIER | c.*2595C>T| |
S18 |
9 | BAA10g05870 | A10 | 3003185 | G | A | downstream_gene_variant | MODIFIER | c.*1047C>T| |
S62 |
10 | BAA10g05870 | A10 | 3003217 | C | T | downstream_gene_variant | MODIFIER | c.*1015G>A| |
S157 S163 |
11 | BAA10g05870 | A10 | 3003525 | C | T | downstream_gene_variant | MODIFIER | c.*707G>A| |
S232 |
12 | BAA10g05870 | A10 | 3003696 | G | A | downstream_gene_variant | MODIFIER | c.*536C>T| |
S290 |
13 | BAA10g05870 | A10 | 3004156 | C | T | downstream_gene_variant | MODIFIER | c.*76G>A| |
S119 |
14 | BAA10g05870 | A10 | 3004503 | G | A | intron_variant | MODIFIER | c.2083-9C>T| |
S264 |
15 | BAA10g05870 | A10 | 3004506 | C | T | intron_variant | MODIFIER | c.2083-12G>A| |
S104 S52 |
16 | BAA10g05870 | A10 | 3005119 | C | T | intron_variant | MODIFIER | c.1949+76G>A| |
S169 |
17 | BAA10g05870 | A10 | 3006249 | G | A | missense_variant | MODERATE | c.1598C>T|p.Pro533Leu |
S19 |
18 | BAA10g05870 | A10 | 3007463 | G | A | splice_region_variant&synonymous_variant | LOW | c.1134C>T|p.Tyr378Tyr |
S262 |
19 | BAA10g05870 | A10 | 3008072 | G | A | missense_variant | MODERATE | c.869C>T|p.Pro290Leu |
S94 |
20 | BAA10g05870 | A10 | 3008591 | G | A | missense_variant | MODERATE | c.512C>T|p.Pro171Leu |
S65 |
21 | BAA10g05870 | A10 | 3009346 | G | A | upstream_gene_variant | MODIFIER | c.-56C>T| |
S117 |
22 | BAA10g05870 | A10 | 3009592 | G | A | upstream_gene_variant | MODIFIER | c.-302C>T| |
S57 |
23 | BAA10g05870 | A10 | 3009789 | C | T | upstream_gene_variant | MODIFIER | c.-499G>A| |
S244 |
24 | BAA10g05870 | A10 | 3011115 | G | A | upstream_gene_variant | MODIFIER | c.-1825C>T| |
S25 |
25 | BAA10g05870 | A10 | 3011325 | C | T | upstream_gene_variant | MODIFIER | c.-2035G>A| |
S15 S4 S6 |