Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19770 | A09 | 12166624 | C | T | downstream_gene_variant | MODIFIER | c.*3216G>A| |
S6 |
2 | BAA09g19770 | A09 | 12167102 | G | A | downstream_gene_variant | MODIFIER | c.*2738C>T| |
S288 |
3 | BAA09g19770 | A09 | 12167116 | G | A | downstream_gene_variant | MODIFIER | c.*2724C>T| |
S301 |
4 | BAA09g19770 | A09 | 12169908 | C | T | missense_variant | MODERATE | c.1738G>A|p.Gly580Ser |
S85 |
5 | BAA09g19770 | A09 | 12170362 | C | T | missense_variant | MODERATE | c.1369G>A|p.Glu457Lys |
S148 S288 |
6 | BAA09g19770 | A09 | 12170650 | C | T | missense_variant | MODERATE | c.1217G>A|p.Arg406Lys |
S150 |
7 | BAA09g19770 | A09 | 12173951 | G | A | intron_variant | MODIFIER | c.529+268C>T| |
S176 |
8 | BAA09g19770 | A09 | 12174096 | C | T | intron_variant | MODIFIER | c.529+123G>A| |
S278 |
9 | BAA09g19770 | A09 | 12174252 | C | T | missense_variant | MODERATE | c.496G>A|p.Val166Ile |
S202 |
10 | BAA09g19770 | A09 | 12175007 | C | T | intron_variant | MODIFIER | c.252+285G>A| |
S37 |
11 | BAA09g19770 | A09 | 12175147 | C | T | intron_variant | MODIFIER | c.252+145G>A| |
S293 |
12 | BAA09g19770 | A09 | 12176277 | G | A | upstream_gene_variant | MODIFIER | c.-734C>T| |
S89 |
13 | BAA09g19770 | A09 | 12176883 | C | T | upstream_gene_variant | MODIFIER | c.-1340G>A| |
S168 |
14 | BAA09g19770 | A09 | 12178641 | G | A | upstream_gene_variant | MODIFIER | c.-3098C>T| |
S1 S90 |
15 | BAA09g19770 | A09 | 12180497 | G | A | upstream_gene_variant | MODIFIER | c.-4954C>T| |
S65 |