| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 93901 | BAA10g03090 | A10 | 1505037 | G | A | missense_variant&splice_region_variant | MODERATE | c.433G>A|p.Val145Ile |
S33 |
| 93902 | BAA10g03090 | A10 | 1506821 | G | A | synonymous_variant | LOW | c.1278G>A|p.Arg426Arg |
S295 |
| 93903 | BAA10g03100 | A10 | 1507943 | C | T | missense_variant | MODERATE | c.2735G>A|p.Gly912Glu |
S166 |
| 93904 | BAA10g03100 | A10 | 1508080 | C | T | synonymous_variant | LOW | c.2598G>A|p.Arg866Arg |
S249 |
| 93905 | BAA10g03110 | A10 | 1508755 | C | T | upstream_gene_variant | MODIFIER | c.-4535C>T| |
S31 |
| 93906 | BAA10g03110 | A10 | 1508766 | C | T | upstream_gene_variant | MODIFIER | c.-4524C>T| |
S166 |
| 93907 | BAA10g03100 | A10 | 1509246 | G | A | missense_variant | MODERATE | c.2059C>T|p.Leu687Phe |
S71 |
| 93908 | BAA10g03100 | A10 | 1509604 | G | A | synonymous_variant | LOW | c.1785C>T|p.Ala595Ala |
S115 |
| 93909 | BAA10g03100 | A10 | 1510797 | C | T | synonymous_variant | LOW | c.690G>A|p.Gln230Gln |
S132 S137 S215 |
| 93910 | BAA10g03110 | A10 | 1511339 | C | T | upstream_gene_variant | MODIFIER | c.-1951C>T| |
S165 |
| 93911 | BAA10g03100 | A10 | 1511465 | C | T | missense_variant | MODERATE | c.514G>A|p.Ala172Thr |
S200 |
| 93912 | BAA10g03100 | A10 | 1511660 | C | T | missense_variant | MODERATE | c.319G>A|p.Val107Met |
S15 S156 S2 S3 S34 |
| 93913 | BAA10g03100 | A10 | 1512425 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S159 S187 S188 S243 S276 |
| 93914 | BAA10g03100 | A10 | 1514229 | G | A | upstream_gene_variant | MODIFIER | c.-2251C>T| |
S198 |
| 93915 | BAA10g03120 | A10 | 1514634 | G | A | synonymous_variant | LOW | c.1137C>T|p.Phe379Phe |
S79 S84 |
| 93916 | BAA10g03120 | A10 | 1514885 | C | T | missense_variant | MODERATE | c.952G>A|p.Gly318Arg |
S35 |
| 93917 | BAA10g03100 | A10 | 1516414 | G | A | upstream_gene_variant | MODIFIER | c.-4436C>T| |
S120 |
| 93918 | BAA10g03120 | A10 | 1518844 | C | T | upstream_gene_variant | MODIFIER | c.-3008G>A| |
S225 |
| 93919 | BAA10g03120 | A10 | 1520693 | G | A | upstream_gene_variant | MODIFIER | c.-4857C>T| |
S187 |
| 93920 | BAA10g03130 | A10 | 1521661 | C | T | downstream_gene_variant | MODIFIER | c.*143G>A| |
S139 |
| 93921 | BAA10g03130 | A10 | 1521853 | C | T | missense_variant | MODERATE | c.1085G>A|p.Ser362Asn |
S272 |
| 93922 | BAA10g03130 | A10 | 1522406 | C | T | missense_variant | MODERATE | c.721G>A|p.Gly241Ser |
S185 |
| 93923 | BAA10g03130 | A10 | 1522515 | C | T | missense_variant | MODERATE | c.694G>A|p.Asp232Asn |
S199 |
| 93924 | BAA10g03130 | A10 | 1524886 | G | A | upstream_gene_variant | MODIFIER | c.-1591C>T| |
S157 S163 |
| 93925 | BAA10g03130 | A10 | 1525073 | G | A | upstream_gene_variant | MODIFIER | c.-1778C>T| |
S306 |