Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g15510 | A09 | 8878431 | G | A | synonymous_variant | LOW | c.2292C>T|p.Ile764Ile |
S249 |
2 | BAA09g15510 | A09 | 8879098 | C | T | splice_region_variant&intron_variant | LOW | c.1893+5G>A| |
S173 |
3 | BAA09g15510 | A09 | 8880262 | C | T | missense_variant | MODERATE | c.1160G>A|p.Arg387Lys |
S168 |
4 | BAA09g15510 | A09 | 8881741 | C | T | intron_variant | MODIFIER | c.825-133G>A| |
S33 |
5 | BAA09g15510 | A09 | 8882002 | G | A | missense_variant | MODERATE | c.757C>T|p.Leu253Phe |
S210 |
6 | BAA09g15510 | A09 | 8882097 | G | A | splice_region_variant&intron_variant | LOW | c.665-3C>T| |
S245 |
7 | BAA09g15510 | A09 | 8882180 | C | T | missense_variant&splice_region_variant | MODERATE | c.664G>A|p.Gly222Arg |
S149 |
8 | BAA09g15510 | A09 | 8882797 | G | A | missense_variant | MODERATE | c.47C>T|p.Ser16Phe |
S130 |
9 | BAA09g15510 | A09 | 8883027 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S270 |
10 | BAA09g15510 | A09 | 8883303 | C | T | upstream_gene_variant | MODIFIER | c.-460G>A| |
S186 |
11 | BAA09g15510 | A09 | 8883686 | C | T | upstream_gene_variant | MODIFIER | c.-843G>A| |
S64 |
12 | BAA09g15510 | A09 | 8884567 | C | T | upstream_gene_variant | MODIFIER | c.-1724G>A| |
S64 |
13 | BAA09g15510 | A09 | 8885102 | C | T | upstream_gene_variant | MODIFIER | c.-2259G>A| |
S10 |
14 | BAA09g15510 | A09 | 8885111 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S130 |
15 | BAA09g15510 | A09 | 8885244 | G | A | upstream_gene_variant | MODIFIER | c.-2401C>T| |
S245 |
16 | BAA09g15510 | A09 | 8885636 | C | T | upstream_gene_variant | MODIFIER | c.-2793G>A| |
S153 |
17 | BAA09g15510 | A09 | 8886468 | G | A | upstream_gene_variant | MODIFIER | c.-3625C>T| |
S44 |
18 | BAA09g15510 | A09 | 8887802 | C | T | upstream_gene_variant | MODIFIER | c.-4959G>A| |
S269 |
19 | BAA09g15510 | A09 | 8887840 | G | A | upstream_gene_variant | MODIFIER | c.-4997C>T| |
S219 S72 |