Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07930 | A10 | 5022068 | C | T | missense_variant | MODERATE | c.785G>A|p.Ser262Asn |
S175 |
2 | BAA10g07930 | A10 | 5022639 | G | A | synonymous_variant | LOW | c.531C>T|p.Ile177Ile |
S289 |
3 | BAA10g07930 | A10 | 5022943 | C | T | synonymous_variant | LOW | c.309G>A|p.Gln103Gln |
S34 |
4 | BAA10g07930 | A10 | 5023189 | G | A | synonymous_variant | LOW | c.135C>T|p.Phe45Phe |
S237 |
5 | BAA10g07930 | A10 | 5023336 | G | A | splice_region_variant&intron_variant | LOW | c.50+8C>T| |
S35 |
6 | BAA10g07930 | A10 | 5023880 | C | T | upstream_gene_variant | MODIFIER | c.-487G>A| |
S34 |
7 | BAA10g07930 | A10 | 5024970 | C | T | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S243 S299 |
8 | BAA10g07930 | A10 | 5025222 | C | T | upstream_gene_variant | MODIFIER | c.-1829G>A| |
S114 |
9 | BAA10g07930 | A10 | 5025560 | G | A | upstream_gene_variant | MODIFIER | c.-2167C>T| |
S138 |
10 | BAA10g07930 | A10 | 5026284 | G | A | upstream_gene_variant | MODIFIER | c.-2891C>T| |
S212 |
11 | BAA10g07930 | A10 | 5027771 | C | T | upstream_gene_variant | MODIFIER | c.-4378G>A| |
S177 |
12 | BAA10g07930 | A10 | 5027989 | C | T | upstream_gene_variant | MODIFIER | c.-4596G>A| |
S180 |
13 | BAA10g07930 | A10 | 5028104 | C | T | upstream_gene_variant | MODIFIER | c.-4711G>A| |
S191 |