| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 128851 | BAA10g16870 | A10 | 16502421 | C | T | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S162 |
| 128852 | BAA10g16870 | A10 | 16503818 | G | A | synonymous_variant | LOW | c.201G>A|p.Gln67Gln |
S57 |
| 128853 | BAA10g16870 | A10 | 16504327 | C | T | missense_variant | MODERATE | c.620C>T|p.Ala207Val |
S68 |
| 128854 | BAA10g16880 | A10 | 16504722 | G | A | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S128 |
| 128855 | BAA10g16870 | A10 | 16504941 | G | A | missense_variant | MODERATE | c.844G>A|p.Asp282Asn |
S36 |
| 128856 | BAA10g16880 | A10 | 16505580 | C | T | upstream_gene_variant | MODIFIER | c.-2041C>T| |
S84 |
| 128857 | BAA10g16880 | A10 | 16506182 | G | A | upstream_gene_variant | MODIFIER | c.-1439G>A| |
S208 S219 |
| 128858 | BAA10g16880 | A10 | 16506484 | C | T | upstream_gene_variant | MODIFIER | c.-1137C>T| |
S232 |
| 128859 | BAA10g16880 | A10 | 16507020 | G | A | upstream_gene_variant | MODIFIER | c.-601G>A| |
S181 |
| 128860 | BAA10g16880 | A10 | 16508504 | C | T | missense_variant | MODERATE | c.343C>T|p.Leu115Phe |
S208 S93 |
| 128861 | BAA10g16890 | A10 | 16508756 | G | A | upstream_gene_variant | MODIFIER | c.-1828G>A| |
S1 S90 |
| 128862 | BAA10g16880 | A10 | 16508862 | G | A | synonymous_variant | LOW | c.507G>A|p.Gln169Gln |
S139 |
| 128863 | BAA10g16880 | A10 | 16509722 | G | A | missense_variant | MODERATE | c.940G>A|p.Glu314Lys |
S64 |
| 128864 | BAA10g16880 | A10 | 16510084 | C | T | missense_variant | MODERATE | c.1151C>T|p.Ser384Leu |
S78 S83 |
| 128865 | BAA10g16890 | A10 | 16511538 | G | A | missense_variant | MODERATE | c.955G>A|p.Asp319Asn |
S40 S49 |
| 128866 | BAA10g16890 | A10 | 16511805 | G | A | missense_variant | MODERATE | c.1222G>A|p.Glu408Lys |
S257 |
| 128867 | BAA10g16900 | A10 | 16513728 | C | T | missense_variant | MODERATE | c.967G>A|p.Val323Ile |
S163 |
| 128868 | BAA10g16900 | A10 | 16513737 | C | T | missense_variant&splice_region_variant | MODERATE | c.958G>A|p.Gly320Ser |
S163 |
| 128869 | BAA10g16900 | A10 | 16514097 | C | T | missense_variant | MODERATE | c.676G>A|p.Val226Ile |
S162 |
| 128870 | BAA10g16900 | A10 | 16516398 | G | A | upstream_gene_variant | MODIFIER | c.-959C>T| |
S27 |
| 128871 | BAA10g16900 | A10 | 16516684 | G | A | upstream_gene_variant | MODIFIER | c.-1245C>T| |
S295 |
| 128872 | BAA10g16920 | A10 | 16519496 | C | T | missense_variant | MODERATE | c.455G>A|p.Arg152Lys |
S156 |
| 128873 | BAA10g16900 | A10 | 16519821 | C | T | upstream_gene_variant | MODIFIER | c.-4382G>A| |
S42 |
| 128874 | BAA10g16910 | A10 | 16521169 | C | T | upstream_gene_variant | MODIFIER | c.-3410G>A| |
S202 |
| 128875 | BAA10g16910 | A10 | 16521848 | G | A | upstream_gene_variant | MODIFIER | c.-4089C>T| |
S280 |