Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g21050 | A08 | 16068856 | G | A | synonymous_variant | LOW | c.909C>T|p.Arg303Arg |
S221 |
2 | BAA08g21050 | A08 | 16068893 | C | T | missense_variant | MODERATE | c.872G>A|p.Ser291Asn |
S33 |
3 | BAA08g21050 | A08 | 16068990 | G | A | missense_variant | MODERATE | c.841C>T|p.His281Tyr |
S162 |
4 | BAA08g21050 | A08 | 16069228 | C | T | missense_variant | MODERATE | c.677G>A|p.Gly226Glu |
S167 |
5 | BAA08g21050 | A08 | 16069632 | C | T | synonymous_variant | LOW | c.597G>A|p.Glu199Glu |
S304 S53 |
6 | BAA08g21050 | A08 | 16070653 | G | A | missense_variant&splice_region_variant | MODERATE | c.310C>T|p.Pro104Ser |
S221 |
7 | BAA08g21050 | A08 | 16070829 | G | A | stop_gained | HIGH | c.208C>T|p.Gln70* |
S204 |
8 | BAA08g21050 | A08 | 16071218 | C | T | missense_variant | MODERATE | c.145G>A|p.Gly49Ser |
S146 S211 |
9 | BAA08g21050 | A08 | 16071226 | G | A | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S155 |
10 | BAA08g21050 | A08 | 16071249 | G | A | synonymous_variant | LOW | c.114C>T|p.Arg38Arg |
S221 |
11 | BAA08g21050 | A08 | 16071266 | C | T | missense_variant | MODERATE | c.97G>A|p.Glu33Lys |
S252 |
12 | BAA08g21050 | A08 | 16073654 | C | T | upstream_gene_variant | MODIFIER | c.-2292G>A| |
S231 |
13 | BAA08g21050 | A08 | 16073830 | C | T | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S2 |