Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10790 | A10 | 12532342 | A | C | downstream_gene_variant | MODIFIER | c.*4917T>G| |
S284 |
2 | BAA10g10790 | A10 | 12532688 | C | T | downstream_gene_variant | MODIFIER | c.*4571G>A| |
S142 |
3 | BAA10g10790 | A10 | 12534489 | C | T | downstream_gene_variant | MODIFIER | c.*2770G>A| |
S5 |
4 | BAA10g10790 | A10 | 12535331 | G | A | downstream_gene_variant | MODIFIER | c.*1928C>T| |
S161 |
5 | BAA10g10790 | A10 | 12535336 | C | T | downstream_gene_variant | MODIFIER | c.*1923G>A| |
S12 |
6 | BAA10g10790 | A10 | 12536859 | C | T | downstream_gene_variant | MODIFIER | c.*400G>A| |
S68 |
7 | BAA10g10790 | A10 | 12537123 | C | G | downstream_gene_variant | MODIFIER | c.*136G>C| |
S104 S131 S136 S157 S178 S207 S258 S275 S283 S286 S289 |
8 | BAA10g10790 | A10 | 12537275 | C | T | missense_variant | MODERATE | c.2081G>A|p.Arg694Lys |
S206 S26 |
9 | BAA10g10790 | A10 | 12537492 | G | A | missense_variant | MODERATE | c.2011C>T|p.Pro671Ser |
S288 |
10 | BAA10g10790 | A10 | 12538365 | C | T | intron_variant | MODIFIER | c.1434-35G>A| |
S70 |
11 | BAA10g10790 | A10 | 12539260 | C | T | missense_variant | MODERATE | c.961G>A|p.Gly321Arg |
S270 |
12 | BAA10g10790 | A10 | 12539884 | G | A | intron_variant | MODIFIER | c.769+23C>T| |
S11 |
13 | BAA10g10790 | A10 | 12539981 | C | T | missense_variant | MODERATE | c.695G>A|p.Gly232Asp |
S117 |
14 | BAA10g10790 | A10 | 12541635 | G | A | intron_variant | MODIFIER | c.562-1521C>T| |
S295 |
15 | BAA10g10790 | A10 | 12541744 | G | A | intron_variant | MODIFIER | c.562-1630C>T| |
S100 |
16 | BAA10g10790 | A10 | 12542066 | G | T | intron_variant | MODIFIER | c.562-1952C>A| |
S221 |
17 | BAA10g10790 | A10 | 12542415 | G | A | intron_variant | MODIFIER | c.562-2301C>T| |
S136 |
18 | BAA10g10790 | A10 | 12542571 | G | A | intron_variant | MODIFIER | c.562-2457C>T| |
S262 |
19 | BAA10g10790 | A10 | 12546001 | G | A | intron_variant | MODIFIER | c.561+3041C>T| |
S184 |
20 | BAA10g10790 | A10 | 12546446 | C | T | intron_variant | MODIFIER | c.561+2596G>A| |
S199 |
21 | BAA10g10790 | A10 | 12547744 | C | T | intron_variant | MODIFIER | c.561+1298G>A| |
S73 S91 |
22 | BAA10g10790 | A10 | 12549434 | G | A | missense_variant | MODERATE | c.169C>T|p.Leu57Phe |
S18 |
23 | BAA10g10790 | A10 | 12549682 | C | T | upstream_gene_variant | MODIFIER | c.-80G>A| |
S144 |
24 | BAA10g10790 | A10 | 12549683 | C | T | upstream_gene_variant | MODIFIER | c.-81G>A| |
S164 |
25 | BAA10g10790 | A10 | 12549883 | G | A | upstream_gene_variant | MODIFIER | c.-281C>T| |
S217 |