Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17060 | A10 | 16601450 | C | T | synonymous_variant | LOW | c.729G>A|p.Val243Val |
S117 |
2 | BAA10g17060 | A10 | 16601566 | C | T | missense_variant | MODERATE | c.613G>A|p.Gly205Ser |
S37 |
3 | BAA10g17060 | A10 | 16601585 | C | T | synonymous_variant | LOW | c.594G>A|p.Glu198Glu |
S249 |
4 | BAA10g17060 | A10 | 16601621 | C | T | synonymous_variant | LOW | c.558G>A|p.Ala186Ala |
S283 |
5 | BAA10g17060 | A10 | 16601854 | A | C | missense_variant | MODERATE | c.325T>G|p.Ser109Ala |
S164 S222 S306 |
6 | BAA10g17060 | A10 | 16601903 | T | G | synonymous_variant | LOW | c.276A>C|p.Pro92Pro |
S126 S170 S208 S240 S245 S250 S265 S295 S304 S4 S88 |
7 | BAA10g17060 | A10 | 16602088 | G | A | missense_variant | MODERATE | c.91C>T|p.Pro31Ser |
S61 |
8 | BAA10g17060 | A10 | 16602525 | C | T | upstream_gene_variant | MODIFIER | c.-347G>A| |
S6 |
9 | BAA10g17060 | A10 | 16604137 | C | A | upstream_gene_variant | MODIFIER | c.-1959G>T| |
S279 |
10 | BAA10g17060 | A10 | 16605024 | G | A | upstream_gene_variant | MODIFIER | c.-2846C>T| |
S241 |