Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g69260 | A09 | 61891285 | G | A | missense_variant&splice_region_variant | MODERATE | c.163G>A|p.Asp55Asn |
S40 S49 |
2 | BAA09g69260 | A09 | 61892575 | C | T | synonymous_variant | LOW | c.1068C>T|p.Leu356Leu |
S305 |
3 | BAA09g69260 | A09 | 61892658 | C | T | missense_variant | MODERATE | c.1151C>T|p.Ser384Leu |
S108 |
4 | BAA09g69260 | A09 | 61892872 | C | T | synonymous_variant | LOW | c.1296C>T|p.Leu432Leu |
S75 S81 |
5 | BAA09g69260 | A09 | 61892938 | C | T | synonymous_variant | LOW | c.1362C>T|p.Ala454Ala |
S176 |
6 | BAA09g69260 | A09 | 61892966 | G | A | missense_variant | MODERATE | c.1390G>A|p.Glu464Lys |
S298 |
7 | BAA09g69260 | A09 | 61892998 | G | A | synonymous_variant | LOW | c.1422G>A|p.Leu474Leu |
S262 |
8 | BAA09g69260 | A09 | 61893043 | C | T | synonymous_variant | LOW | c.1467C>T|p.Pro489Pro |
S103 |