Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g16860 | A09 | 9964764 | C | T | upstream_gene_variant | MODIFIER | c.-3403C>T| |
S182 |
2 | BAA09g16860 | A09 | 9965226 | G | A | upstream_gene_variant | MODIFIER | c.-2941G>A| |
S249 |
3 | BAA09g16860 | A09 | 9967545 | G | A | upstream_gene_variant | MODIFIER | c.-622G>A| |
S162 |
4 | BAA09g16860 | A09 | 9968448 | C | T | synonymous_variant | LOW | c.210C>T|p.Asn70Asn |
S2 |
5 | BAA09g16860 | A09 | 9968595 | C | T | missense_variant | MODERATE | c.275C>T|p.Ser92Leu |
S303 |
6 | BAA09g16860 | A09 | 9970571 | C | T | synonymous_variant | LOW | c.1158C>T|p.Cys386Cys |
S33 |
7 | BAA09g16860 | A09 | 9970640 | G | A | synonymous_variant | LOW | c.1227G>A|p.Arg409Arg |
S280 |
8 | BAA09g16860 | A09 | 9970807 | G | A | missense_variant | MODERATE | c.1394G>A|p.Arg465Lys |
S233 |
9 | BAA09g16860 | A09 | 9971004 | G | A | intron_variant | MODIFIER | c.1582+9G>A| |
S239 |
10 | BAA09g16860 | A09 | 9971205 | G | A | missense_variant | MODERATE | c.1705G>A|p.Ala569Thr |
S74 |
11 | BAA09g16860 | A09 | 9971894 | G | A | intron_variant | MODIFIER | c.2086+150G>A| |
S99 |
12 | BAA09g16860 | A09 | 9972421 | C | T | intron_variant | MODIFIER | c.2323-54C>T| |
S278 |
13 | BAA09g16860 | A09 | 9975054 | G | A | downstream_gene_variant | MODIFIER | c.*2148G>A| |
S225 |
14 | BAA09g16860 | A09 | 9975221 | C | T | downstream_gene_variant | MODIFIER | c.*2315C>T| |
S104 S52 |
15 | BAA09g16860 | A09 | 9976210 | C | T | downstream_gene_variant | MODIFIER | c.*3304C>T| |
S150 |
16 | BAA09g16860 | A09 | 9976419 | G | A | downstream_gene_variant | MODIFIER | c.*3513G>A| |
S189 |
17 | BAA09g16860 | A09 | 9976632 | C | T | downstream_gene_variant | MODIFIER | c.*3726C>T| |
S156 S2 |
18 | BAA09g16860 | A09 | 9976684 | C | T | downstream_gene_variant | MODIFIER | c.*3778C>T| |
S292 |