Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g36060 | A07 | 33883824 | C | T | missense_variant | MODERATE | c.598C>T|p.Arg200Cys |
S265 |
2 | BAA07g36060 | A07 | 33884525 | C | T | synonymous_variant | LOW | c.1221C>T|p.Leu407Leu |
S174 S216 S241 S27 |
3 | BAA07g36060 | A07 | 33884671 | C | T | missense_variant | MODERATE | c.1367C>T|p.Ser456Phe |
S71 |
4 | BAA07g36060 | A07 | 33884686 | G | A | missense_variant | MODERATE | c.1382G>A|p.Gly461Glu |
S301 S304 |
5 | BAA07g36060 | A07 | 33885190 | G | A | missense_variant | MODERATE | c.1810G>A|p.Asp604Asn |
S136 |
6 | BAA07g36060 | A07 | 33885277 | G | A | missense_variant | MODERATE | c.1897G>A|p.Asp633Asn |
S171 |
7 | BAA07g36060 | A07 | 33885613 | C | T | missense_variant | MODERATE | c.2233C>T|p.His745Tyr |
S269 |
8 | BAA07g36060 | A07 | 33885727 | C | T | synonymous_variant | LOW | c.2347C>T|p.Leu783Leu |
S162 |
9 | BAA07g36060 | A07 | 33887161 | C | T | synonymous_variant | LOW | c.3231C>T|p.Val1077Val |
S193 |
10 | BAA07g36060 | A07 | 33887968 | G | A | synonymous_variant | LOW | c.4038G>A|p.Lys1346Lys |
S288 |