Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21190 | A10 | 18717885 | G | A | missense_variant | MODERATE | c.1682C>T|p.Ser561Phe |
S182 |
2 | BAA10g21190 | A10 | 18718291 | G | A | missense_variant | MODERATE | c.1444C>T|p.Pro482Ser |
S181 |
3 | BAA10g21190 | A10 | 18718450 | C | T | missense_variant | MODERATE | c.1373G>A|p.Gly458Glu |
S275 |
4 | BAA10g21190 | A10 | 18718477 | G | A | missense_variant | MODERATE | c.1346C>T|p.Thr449Ile |
S18 |
5 | BAA10g21190 | A10 | 18718921 | C | T | synonymous_variant | LOW | c.1077G>A|p.Leu359Leu |
S244 |
6 | BAA10g21190 | A10 | 18719171 | C | T | missense_variant | MODERATE | c.1018G>A|p.Asp340Asn |
S247 |
7 | BAA10g21190 | A10 | 18719593 | G | A | missense_variant | MODERATE | c.766C>T|p.Pro256Ser |
S42 |
8 | BAA10g21190 | A10 | 18719650 | G | A | synonymous_variant | LOW | c.709C>T|p.Leu237Leu |
S17 |
9 | BAA10g21190 | A10 | 18722559 | G | A | upstream_gene_variant | MODIFIER | c.-1780C>T| |
S271 |
10 | BAA10g21190 | A10 | 18723469 | C | T | upstream_gene_variant | MODIFIER | c.-2690G>A| |
S173 |
11 | BAA10g21190 | A10 | 18724154 | G | A | upstream_gene_variant | MODIFIER | c.-3375C>T| |
S103 |
12 | BAA10g21190 | A10 | 18724934 | T | A | upstream_gene_variant | MODIFIER | c.-4155A>T| |
S206 |
13 | BAA10g21190 | A10 | 18725544 | C | T | upstream_gene_variant | MODIFIER | c.-4765G>A| |
S189 |