Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53570 | A09 | 54765211 | C | T | missense_variant | MODERATE | c.62C>T|p.Ser21Phe |
S186 |
2 | BAA09g53570 | A09 | 54765266 | C | T | synonymous_variant | LOW | c.117C>T|p.Asn39Asn |
S278 |
3 | BAA09g53570 | A09 | 54766136 | C | T | splice_region_variant&intron_variant | LOW | c.438-3C>T| |
S192 |
4 | BAA09g53570 | A09 | 54766676 | G | A | missense_variant | MODERATE | c.670G>A|p.Glu224Lys |
S17 |
5 | BAA09g53570 | A09 | 54767563 | C | T | missense_variant | MODERATE | c.1013C>T|p.Pro338Leu |
S183 |
6 | BAA09g53570 | A09 | 54767621 | C | T | synonymous_variant | LOW | c.1071C>T|p.Tyr357Tyr |
S293 |
7 | BAA09g53570 | A09 | 54767996 | G | A | synonymous_variant | LOW | c.1344G>A|p.Gln448Gln |
S265 |
8 | BAA09g53570 | A09 | 54768421 | G | A | missense_variant | MODERATE | c.1640G>A|p.Arg547His |
S172 S217 |
9 | BAA09g53570 | A09 | 54769311 | C | T | missense_variant | MODERATE | c.2434C>T|p.Leu812Phe |
S208 S219 |
10 | BAA09g53570 | A09 | 54769810 | G | A | synonymous_variant | LOW | c.2751G>A|p.Val917Val |
S210 S225 |
11 | BAA09g53570 | A09 | 54769857 | C | T | missense_variant | MODERATE | c.2798C>T|p.Ala933Val |
S61 |