Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g28120 | A10 | 21661227 | C | T | missense_variant | MODERATE | c.2461G>A|p.Glu821Lys |
S265 |
2 | BAA10g28120 | A10 | 21661554 | C | T | missense_variant&splice_region_variant | MODERATE | c.2197G>A|p.Val733Ile |
S177 |
3 | BAA10g28120 | A10 | 21661917 | C | T | missense_variant | MODERATE | c.2020G>A|p.Glu674Lys |
S82 S92 |
4 | BAA10g28120 | A10 | 21665011 | C | T | intron_variant | MODIFIER | c.105+18G>A| |
S48 |
5 | BAA10g28120 | A10 | 21665445 | C | T | upstream_gene_variant | MODIFIER | c.-312G>A| |
S218 |
6 | BAA10g28120 | A10 | 21666748 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S200 |
7 | BAA10g28120 | A10 | 21667287 | G | A | upstream_gene_variant | MODIFIER | c.-2154C>T| |
S90 |
8 | BAA10g28120 | A10 | 21668052 | C | T | upstream_gene_variant | MODIFIER | c.-2919G>A| |
S281 |
9 | BAA10g28120 | A10 | 21669804 | C | T | upstream_gene_variant | MODIFIER | c.-4671G>A| |
S87 |
10 | BAA10g28120 | A10 | 21669906 | G | A | upstream_gene_variant | MODIFIER | c.-4773C>T| |
S176 |