Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02020 | A10 | 964446 | G | A | missense_variant | MODERATE | c.40G>A|p.Gly14Arg |
S5 |
2 | BAA10g02020 | A10 | 964620 | G | A | missense_variant | MODERATE | c.214G>A|p.Glu72Lys |
S303 |
3 | BAA10g02020 | A10 | 964964 | G | A | synonymous_variant | LOW | c.558G>A|p.Arg186Arg |
S293 |
4 | BAA10g02020 | A10 | 965084 | T | A | synonymous_variant | LOW | c.678T>A|p.Ile226Ile |
S38 |
5 | BAA10g02020 | A10 | 965117 | C | T | synonymous_variant | LOW | c.711C>T|p.Asn237Asn |
S269 |
6 | BAA10g02020 | A10 | 966673 | G | A | missense_variant | MODERATE | c.935G>A|p.Arg312Lys |
S18 |
7 | BAA10g02020 | A10 | 966721 | C | T | missense_variant | MODERATE | c.983C>T|p.Ser328Leu |
S40 S49 |
8 | BAA10g02020 | A10 | 966854 | C | T | synonymous_variant | LOW | c.1116C>T|p.Asn372Asn |
S199 |
9 | BAA10g02020 | A10 | 967190 | G | A | synonymous_variant | LOW | c.1452G>A|p.Glu484Glu |
S171 |
10 | BAA10g02020 | A10 | 967271 | G | A | synonymous_variant | LOW | c.1533G>A|p.Gln511Gln |
S97 |
11 | BAA10g02020 | A10 | 967484 | G | A | synonymous_variant | LOW | c.1746G>A|p.Ala582Ala |
S40 S49 |
12 | BAA10g02020 | A10 | 967821 | G | A | missense_variant | MODERATE | c.2083G>A|p.Glu695Lys |
S236 |
13 | BAA10g02020 | A10 | 967909 | G | A | missense_variant | MODERATE | c.2171G>A|p.Gly724Glu |
S59 |