| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 91751 | BAA10g01660 | A10 | 805579 | G | T | missense_variant | MODERATE | c.484C>A|p.His162Asn |
S147 S91 |
| 91752 | BAA10g01660 | A10 | 805584 | C | G | missense_variant | MODERATE | c.479G>C|p.Cys160Ser |
S147 S91 |
| 91753 | BAA10g01660 | A10 | 805598 | A | G | synonymous_variant | LOW | c.465T>C|p.Ser155Ser |
S147 S91 |
| 91754 | BAA10g01640 | A10 | 806047 | G | A | upstream_gene_variant | MODIFIER | c.-4314C>T| |
S38 |
| 91755 | BAA10g01660 | A10 | 806093 | C | T | missense_variant&splice_region_variant | MODERATE | c.199G>A|p.Glu67Lys |
S70 |
| 91756 | BAA10g01670 | A10 | 807079 | G | A | missense_variant | MODERATE | c.691C>T|p.Pro231Ser |
S153 S213 |
| 91757 | BAA10g01670 | A10 | 807397 | C | T | missense_variant | MODERATE | c.373G>A|p.Glu125Lys |
S252 |
| 91758 | BAA10g01670 | A10 | 807463 | C | T | missense_variant | MODERATE | c.307G>A|p.Glu103Lys |
S206 S26 |
| 91759 | BAA10g01650 | A10 | 808765 | C | T | upstream_gene_variant | MODIFIER | c.-4566G>A| |
S182 |
| 91760 | BAA10g01650 | A10 | 809129 | G | A | upstream_gene_variant | MODIFIER | c.-4930C>T| |
S153 S213 |
| 91761 | BAA10g01660 | A10 | 810107 | C | T | upstream_gene_variant | MODIFIER | c.-3717G>A| |
S173 |
| 91762 | BAA10g01660 | A10 | 810833 | C | T | upstream_gene_variant | MODIFIER | c.-4443G>A| |
S155 |
| 91763 | BAA10g01670 | A10 | 811443 | C | T | upstream_gene_variant | MODIFIER | c.-3129G>A| |
S149 |
| 91764 | BAA10g01670 | A10 | 811819 | G | A | upstream_gene_variant | MODIFIER | c.-3505C>T| |
S1 S90 |
| 91765 | BAA10g01670 | A10 | 811932 | G | A | upstream_gene_variant | MODIFIER | c.-3618C>T| |
S120 |
| 91766 | BAA10g01670 | A10 | 812579 | G | A | upstream_gene_variant | MODIFIER | c.-4265C>T| |
S308 |
| 91767 | BAA10g01690 | A10 | 813280 | C | T | synonymous_variant | LOW | c.684G>A|p.Glu228Glu |
S281 |
| 91768 | BAA10g01690 | A10 | 813295 | G | A | synonymous_variant | LOW | c.669C>T|p.Arg223Arg |
S157 S163 |
| 91769 | BAA10g01690 | A10 | 813632 | C | T | missense_variant | MODERATE | c.332G>A|p.Arg111Lys |
S226 |
| 91770 | BAA10g01700 | A10 | 817619 | G | T | missense_variant | MODERATE | c.494G>T|p.Gly165Val |
S184 |
| 91771 | BAA10g01700 | A10 | 818974 | C | T | missense_variant | MODERATE | c.1628C>T|p.Ser543Phe |
S110 |
| 91772 | BAA10g01700 | A10 | 819300 | C | T | missense_variant | MODERATE | c.1879C>T|p.Leu627Phe |
S34 |
| 91773 | BAA10g01700 | A10 | 819515 | G | A | missense_variant | MODERATE | c.2021G>A|p.Arg674Lys |
S217 S248 |
| 91774 | BAA10g01710 | A10 | 820668 | G | A | upstream_gene_variant | MODIFIER | c.-1703G>A| |
S211 |
| 91775 | BAA10g01710 | A10 | 822788 | C | T | synonymous_variant | LOW | c.342C>T|p.Phe114Phe |
S42 |