Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19420 | A10 | 17804736 | G | A | missense_variant | MODERATE | c.1082C>T|p.Ser361Leu |
S240 |
2 | BAA10g19420 | A10 | 17804879 | G | A | synonymous_variant | LOW | c.939C>T|p.Arg313Arg |
S127 |
3 | BAA10g19420 | A10 | 17804997 | G | A | missense_variant | MODERATE | c.821C>T|p.Ser274Leu |
S217 |
4 | BAA10g19420 | A10 | 17805107 | C | T | synonymous_variant | LOW | c.783G>A|p.Lys261Lys |
S18 |
5 | BAA10g19420 | A10 | 17806247 | G | A | missense_variant | MODERATE | c.146C>T|p.Thr49Ile |
S195 |
6 | BAA10g19420 | A10 | 17806252 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.142-1G>A| |
S99 |
7 | BAA10g19420 | A10 | 17807764 | G | A | upstream_gene_variant | MODIFIER | c.-1179C>T| |
S163 |
8 | BAA10g19420 | A10 | 17808125 | C | T | upstream_gene_variant | MODIFIER | c.-1540G>A| |
S26 |
9 | BAA10g19420 | A10 | 17808252 | C | T | upstream_gene_variant | MODIFIER | c.-1667G>A| |
S146 |
10 | BAA10g19420 | A10 | 17808597 | G | A | upstream_gene_variant | MODIFIER | c.-2012C>T| |
S128 |
11 | BAA10g19420 | A10 | 17809054 | C | T | upstream_gene_variant | MODIFIER | c.-2469G>A| |
S203 |
12 | BAA10g19420 | A10 | 17809152 | C | T | upstream_gene_variant | MODIFIER | c.-2567G>A| |
S60 |
13 | BAA10g19420 | A10 | 17810205 | G | A | upstream_gene_variant | MODIFIER | c.-3620C>T| |
S288 |
14 | BAA10g19420 | A10 | 17810274 | C | T | upstream_gene_variant | MODIFIER | c.-3689G>A| |
S56 |
15 | BAA10g19420 | A10 | 17811514 | G | A | upstream_gene_variant | MODIFIER | c.-4929C>T| |
S158 |