Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14550 | A08 | 12386128 | C | T | missense_variant | MODERATE | c.428C>T|p.Ser143Phe |
S135 |
2 | BAA08g14550 | A08 | 12388508 | G | A | missense_variant | MODERATE | c.1196G>A|p.Gly399Glu |
S236 |
3 | BAA08g14550 | A08 | 12390099 | C | T | splice_region_variant&intron_variant | LOW | c.1873-8C>T| |
S308 |
4 | BAA08g14550 | A08 | 12390352 | C | T | synonymous_variant | LOW | c.2118C>T|p.Pro706Pro |
S216 |
5 | BAA08g14550 | A08 | 12391008 | G | A | missense_variant | MODERATE | c.2596G>A|p.Glu866Lys |
S131 |
6 | BAA08g14550 | A08 | 12391327 | G | A | missense_variant | MODERATE | c.2821G>A|p.Ala941Thr |
S32 |
7 | BAA08g14550 | A08 | 12391835 | G | A | missense_variant | MODERATE | c.3232G>A|p.Val1078Ile |
S286 |
8 | BAA08g14550 | A08 | 12392144 | G | A | missense_variant | MODERATE | c.3541G>A|p.Asp1181Asn |
S269 |
9 | BAA08g14550 | A08 | 12392186 | G | A | missense_variant | MODERATE | c.3583G>A|p.Asp1195Asn |
S72 S78 |
10 | BAA08g14550 | A08 | 12395073 | C | T | downstream_gene_variant | MODIFIER | c.*2831C>T| |
S58 |
11 | BAA08g14550 | A08 | 12395464 | G | A | downstream_gene_variant | MODIFIER | c.*3222G>A| |
S280 |