Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g53290 | A03 | 26220600 | C | T | missense_variant | MODERATE | c.2321G>A|p.Gly774Glu |
S201 |
2 | BAA03g53290 | A03 | 26220883 | C | T | missense_variant | MODERATE | c.2038G>A|p.Asp680Asn |
S158 |
3 | BAA03g53290 | A03 | 26220985 | C | T | missense_variant | MODERATE | c.1936G>A|p.Ala646Thr |
S176 |
4 | BAA03g53290 | A03 | 26221207 | G | A | missense_variant | MODERATE | c.1714C>T|p.Leu572Phe |
S95 |
5 | BAA03g53290 | A03 | 26221914 | C | T | missense_variant | MODERATE | c.1181G>A|p.Gly394Asp |
S293 |
6 | BAA03g53290 | A03 | 26222797 | C | T | missense_variant | MODERATE | c.298G>A|p.Gly100Arg |
S131 |
7 | BAA03g53290 | A03 | 26223612 | G | A | intron_variant | MODIFIER | c.193-710C>T| |
S48 |
8 | BAA03g53290 | A03 | 26224004 | C | T | intron_variant | MODIFIER | c.192+478G>A| |
S23 |
9 | BAA03g53290 | A03 | 26224245 | C | T | intron_variant | MODIFIER | c.192+237G>A| |
S114 |
10 | BAA03g53290 | A03 | 26224627 | G | A | missense_variant | MODERATE | c.47C>T|p.Ser16Phe |
S218 |
11 | BAA03g53290 | A03 | 26226463 | C | T | upstream_gene_variant | MODIFIER | c.-1790G>A| |
S306 S308 |
12 | BAA03g53290 | A03 | 26226572 | C | T | upstream_gene_variant | MODIFIER | c.-1899G>A| |
S40 S49 |
13 | BAA03g53290 | A03 | 26227259 | C | T | upstream_gene_variant | MODIFIER | c.-2586G>A| |
S92 |