Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14270 | A10 | 15058750 | G | A | upstream_gene_variant | MODIFIER | c.-4344G>A| |
S172 S217 |
2 | BAA10g14270 | A10 | 15058880 | C | T | upstream_gene_variant | MODIFIER | c.-4214C>T| |
S185 |
3 | BAA10g14270 | A10 | 15058887 | C | T | upstream_gene_variant | MODIFIER | c.-4207C>T| |
S283 |
4 | BAA10g14270 | A10 | 15059133 | G | A | upstream_gene_variant | MODIFIER | c.-3961G>A| |
S207 |
5 | BAA10g14270 | A10 | 15059138 | G | A | upstream_gene_variant | MODIFIER | c.-3956G>A| |
S205 |
6 | BAA10g14270 | A10 | 15059888 | G | A | upstream_gene_variant | MODIFIER | c.-3206G>A| |
S276 |
7 | BAA10g14270 | A10 | 15059952 | G | A | upstream_gene_variant | MODIFIER | c.-3142G>A| |
S43 |
8 | BAA10g14270 | A10 | 15063159 | C | T | synonymous_variant | LOW | c.66C>T|p.Phe22Phe |
S20 |
9 | BAA10g14270 | A10 | 15063532 | C | T | splice_region_variant&intron_variant | LOW | c.264+6C>T| |
S33 |
10 | BAA10g14270 | A10 | 15063824 | C | T | missense_variant | MODERATE | c.484C>T|p.Arg162Trp |
S99 |
11 | BAA10g14270 | A10 | 15064369 | G | A | missense_variant | MODERATE | c.760G>A|p.Ala254Thr |
S221 |