Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g31700 | A10 | 23039865 | G | A | intron_variant | MODIFIER | c.2098-410C>T| |
S205 |
2 | BAA10g31700 | A10 | 23039944 | G | A | intron_variant | MODIFIER | c.2098-489C>T| |
S241 |
3 | BAA10g31700 | A10 | 23043463 | G | A | stop_gained | HIGH | c.2014C>T|p.Gln672* |
S35 |
4 | BAA10g31700 | A10 | 23043836 | G | A | missense_variant | MODERATE | c.1717C>T|p.Pro573Ser |
S174 |
5 | BAA10g31700 | A10 | 23043890 | C | T | missense_variant | MODERATE | c.1663G>A|p.Glu555Lys |
S146 |
6 | BAA10g31700 | A10 | 23043947 | C | T | missense_variant | MODERATE | c.1606G>A|p.Ala536Thr |
S302 |
7 | BAA10g31700 | A10 | 23044311 | C | T | splice_region_variant&intron_variant | LOW | c.1596+5G>A| |
S236 |
8 | BAA10g31700 | A10 | 23044747 | G | A | missense_variant | MODERATE | c.1165C>T|p.Pro389Ser |
S216 |
9 | BAA10g31700 | A10 | 23044969 | C | T | missense_variant | MODERATE | c.943G>A|p.Val315Ile |
S12 |
10 | BAA10g31700 | A10 | 23045074 | C | T | missense_variant | MODERATE | c.838G>A|p.Asp280Asn |
S169 |
11 | BAA10g31700 | A10 | 23045134 | C | T | missense_variant | MODERATE | c.778G>A|p.Asp260Asn |
S230 |
12 | BAA10g31700 | A10 | 23046474 | C | T | upstream_gene_variant | MODIFIER | c.-334G>A| |
S129 |
13 | BAA10g31700 | A10 | 23046540 | C | T | upstream_gene_variant | MODIFIER | c.-400G>A| |
S90 |
14 | BAA10g31700 | A10 | 23048102 | G | A | upstream_gene_variant | MODIFIER | c.-1962C>T| |
S151 |
15 | BAA10g31700 | A10 | 23048519 | C | T | upstream_gene_variant | MODIFIER | c.-2379G>A| |
S25 |
16 | BAA10g31700 | A10 | 23049562 | G | A | upstream_gene_variant | MODIFIER | c.-3422C>T| |
S217 |
17 | BAA10g31700 | A10 | 23049701 | C | T | upstream_gene_variant | MODIFIER | c.-3561G>A| |
S12 |
18 | BAA10g31700 | A10 | 23049866 | G | A | upstream_gene_variant | MODIFIER | c.-3726C>T| |
S171 |