Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01980 | A10 | 944682 | C | T | upstream_gene_variant | MODIFIER | c.-2249C>T| |
S63 |
2 | BAA10g01980 | A10 | 944887 | G | A | upstream_gene_variant | MODIFIER | c.-2044G>A| |
S211 S227 |
3 | BAA10g01980 | A10 | 947227 | G | A | missense_variant&splice_region_variant | MODERATE | c.205G>A|p.Val69Ile |
S172 S217 |
4 | BAA10g01980 | A10 | 947437 | C | T | missense_variant | MODERATE | c.305C>T|p.Ser102Leu |
S221 |
5 | BAA10g01980 | A10 | 947612 | G | A | synonymous_variant | LOW | c.480G>A|p.Lys160Lys |
S280 |
6 | BAA10g01980 | A10 | 947714 | C | T | synonymous_variant | LOW | c.582C>T|p.Val194Val |
S12 |
7 | BAA10g01980 | A10 | 947746 | G | A | missense_variant | MODERATE | c.614G>A|p.Gly205Asp |
S237 |
8 | BAA10g01980 | A10 | 947923 | C | T | missense_variant | MODERATE | c.791C>T|p.Ser264Leu |
S25 |
9 | BAA10g01980 | A10 | 948663 | C | T | missense_variant | MODERATE | c.1304C>T|p.Ser435Phe |
S281 |
10 | BAA10g01980 | A10 | 948766 | G | A | missense_variant | MODERATE | c.1327G>A|p.Asp443Asn |
S83 S88 |
11 | BAA10g01980 | A10 | 952190 | G | A | downstream_gene_variant | MODIFIER | c.*3018G>A| |
S80 |
12 | BAA10g01980 | A10 | 952561 | C | T | downstream_gene_variant | MODIFIER | c.*3389C>T| |
S23 |
13 | BAA10g01980 | A10 | 952937 | G | A | downstream_gene_variant | MODIFIER | c.*3765G>A| |
S48 |
14 | BAA10g01980 | A10 | 953143 | G | A | downstream_gene_variant | MODIFIER | c.*3971G>A| |
S4 |
15 | BAA10g01980 | A10 | 953176 | C | T | downstream_gene_variant | MODIFIER | c.*4004C>T| |
S87 |
16 | BAA10g01980 | A10 | 953773 | G | A | downstream_gene_variant | MODIFIER | c.*4601G>A| |
S189 |