Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19190 | A10 | 17690406 | C | T | synonymous_variant | LOW | c.4392G>A|p.Pro1464Pro |
S191 |
2 | BAA10g19190 | A10 | 17690454 | G | A | synonymous_variant | LOW | c.4344C>T|p.Phe1448Phe |
S288 |
3 | BAA10g19190 | A10 | 17690624 | C | T | missense_variant | MODERATE | c.4174G>A|p.Val1392Ile |
S86 |
4 | BAA10g19190 | A10 | 17690792 | C | T | missense_variant | MODERATE | c.4006G>A|p.Val1336Met |
S277 |
5 | BAA10g19190 | A10 | 17691445 | C | T | missense_variant | MODERATE | c.3353G>A|p.Arg1118Lys |
S177 |
6 | BAA10g19190 | A10 | 17691643 | G | A | missense_variant | MODERATE | c.3155C>T|p.Thr1052Ile |
S75 S81 |
7 | BAA10g19190 | A10 | 17694632 | G | A | synonymous_variant | LOW | c.166C>T|p.Leu56Leu |
S160 |
8 | BAA10g19190 | A10 | 17694767 | C | T | missense_variant | MODERATE | c.31G>A|p.Asp11Asn |
S18 |
9 | BAA10g19190 | A10 | 17694901 | G | A | upstream_gene_variant | MODIFIER | c.-104C>T| |
S158 |
10 | BAA10g19190 | A10 | 17694917 | G | A | upstream_gene_variant | MODIFIER | c.-120C>T| |
S195 |
11 | BAA10g19190 | A10 | 17695265 | G | A | upstream_gene_variant | MODIFIER | c.-468C>T| |
S197 |
12 | BAA10g19190 | A10 | 17696358 | C | T | upstream_gene_variant | MODIFIER | c.-1561G>A| |
S52 |
13 | BAA10g19190 | A10 | 17696452 | G | A | upstream_gene_variant | MODIFIER | c.-1655C>T| |
S295 |