Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g17430 | A08 | 14230775 | C | T | synonymous_variant | LOW | c.2214G>A|p.Lys738Lys |
S159 |
2 | BAA08g17430 | A08 | 14230927 | C | T | missense_variant | MODERATE | c.2062G>A|p.Val688Ile |
S67 |
3 | BAA08g17430 | A08 | 14231635 | C | T | missense_variant | MODERATE | c.1354G>A|p.Val452Ile |
S167 |
4 | BAA08g17430 | A08 | 14231872 | C | T | missense_variant | MODERATE | c.1117G>A|p.Glu373Lys |
S228 |
5 | BAA08g17430 | A08 | 14232118 | G | A | stop_gained | HIGH | c.871C>T|p.Gln291* |
S260 |
6 | BAA08g17430 | A08 | 14232212 | C | T | stop_gained | HIGH | c.777G>A|p.Trp259* |
S45 |
7 | BAA08g17430 | A08 | 14232655 | C | T | missense_variant | MODERATE | c.334G>A|p.Glu112Lys |
S305 |
8 | BAA08g17430 | A08 | 14232732 | G | A | missense_variant | MODERATE | c.257C>T|p.Ala86Val |
S292 |
9 | BAA08g17430 | A08 | 14234098 | C | T | upstream_gene_variant | MODIFIER | c.-1110G>A| |
S159 |
10 | BAA08g17430 | A08 | 14234331 | G | A | upstream_gene_variant | MODIFIER | c.-1343C>T| |
S229 |
11 | BAA08g17430 | A08 | 14234901 | G | A | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S221 |
12 | BAA08g17430 | A08 | 14236049 | C | T | upstream_gene_variant | MODIFIER | c.-3061G>A| |
S251 |
13 | BAA08g17430 | A08 | 14236750 | G | A | upstream_gene_variant | MODIFIER | c.-3762C>T| |
S249 |