Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08000 | A10 | 5110394 | C | T | downstream_gene_variant | MODIFIER | c.*1271G>A| |
S195 |
2 | BAA10g08000 | A10 | 5110652 | G | A | downstream_gene_variant | MODIFIER | c.*1013C>T| |
S161 |
3 | BAA10g08000 | A10 | 5111204 | G | A | downstream_gene_variant | MODIFIER | c.*461C>T| |
S125 |
4 | BAA10g08000 | A10 | 5112450 | G | A | synonymous_variant | LOW | c.946C>T|p.Leu316Leu |
S201 |
5 | BAA10g08000 | A10 | 5112640 | C | T | synonymous_variant | LOW | c.756G>A|p.Gly252Gly |
S92 |
6 | BAA10g08000 | A10 | 5112689 | G | A | missense_variant | MODERATE | c.707C>T|p.Ser236Leu |
S18 |
7 | BAA10g08000 | A10 | 5113061 | G | A | missense_variant | MODERATE | c.335C>T|p.Pro112Leu |
S3 |
8 | BAA10g08000 | A10 | 5113526 | G | A | upstream_gene_variant | MODIFIER | c.-131C>T| |
S303 |
9 | BAA10g08000 | A10 | 5114502 | C | T | upstream_gene_variant | MODIFIER | c.-1107G>A| |
S247 |
10 | BAA10g08000 | A10 | 5114534 | G | A | upstream_gene_variant | MODIFIER | c.-1139C>T| |
S236 |
11 | BAA10g08000 | A10 | 5114649 | G | A | upstream_gene_variant | MODIFIER | c.-1254C>T| |
S236 |
12 | BAA10g08000 | A10 | 5115066 | G | A | upstream_gene_variant | MODIFIER | c.-1671C>T| |
S283 |
13 | BAA10g08000 | A10 | 5116886 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S176 |
14 | BAA10g08000 | A10 | 5116897 | C | T | upstream_gene_variant | MODIFIER | c.-3502G>A| |
S98 |
15 | BAA10g08000 | A10 | 5117109 | G | A | upstream_gene_variant | MODIFIER | c.-3714C>T| |
S174 S216 S241 S265 S39 |
16 | BAA10g08000 | A10 | 5117493 | C | T | upstream_gene_variant | MODIFIER | c.-4098G>A| |
S269 |
17 | BAA10g08000 | A10 | 5117918 | G | A | upstream_gene_variant | MODIFIER | c.-4523C>T| |
S158 |