| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 91651 | BAA10g01570 | A10 | 773195 | G | A | upstream_gene_variant | MODIFIER | c.-1499C>T| |
S283 |
| 91652 | BAA10g01590 | A10 | 773479 | C | T | missense_variant | MODERATE | c.73C>T|p.Arg25Cys |
S249 |
| 91653 | BAA10g01570 | A10 | 773768 | C | T | upstream_gene_variant | MODIFIER | c.-2072G>A| |
S196 |
| 91654 | BAA10g01570 | A10 | 775301 | C | T | upstream_gene_variant | MODIFIER | c.-3605G>A| |
S221 |
| 91655 | BAA10g01590 | A10 | 775877 | C | T | missense_variant | MODERATE | c.550C>T|p.Leu184Phe |
S34 |
| 91656 | BAA10g01590 | A10 | 776521 | G | A | missense_variant | MODERATE | c.947G>A|p.Ser316Asn |
S192 |
| 91657 | BAA10g01590 | A10 | 776551 | G | A | missense_variant | MODERATE | c.977G>A|p.Ser326Asn |
S158 |
| 91658 | BAA10g01600 | A10 | 778069 | C | T | upstream_gene_variant | MODIFIER | c.-2439C>T| |
S305 |
| 91659 | BAA10g01600 | A10 | 778498 | G | A | upstream_gene_variant | MODIFIER | c.-2010G>A| |
S203 |
| 91660 | BAA10g01600 | A10 | 778543 | C | T | upstream_gene_variant | MODIFIER | c.-1965C>T| |
S288 |
| 91661 | BAA10g01590 | A10 | 780702 | C | T | downstream_gene_variant | MODIFIER | c.*3054C>T| |
S235 |
| 91662 | BAA10g01590 | A10 | 781402 | C | T | downstream_gene_variant | MODIFIER | c.*3754C>T| |
S110 |
| 91663 | BAA10g01610 | A10 | 783090 | C | T | missense_variant | MODERATE | c.331G>A|p.Glu111Lys |
S175 |
| 91664 | BAA10g01610 | A10 | 784067 | C | T | upstream_gene_variant | MODIFIER | c.-647G>A| |
S241 S39 |
| 91665 | BAA10g01620 | A10 | 784533 | G | A | synonymous_variant | LOW | c.480C>T|p.Ala160Ala |
S109 |
| 91666 | BAA10g01620 | A10 | 784836 | C | T | splice_donor_variant&intron_variant | HIGH | c.352+1G>A| |
S174 S98 |
| 91667 | BAA10g01610 | A10 | 786300 | G | A | upstream_gene_variant | MODIFIER | c.-2880C>T| |
S234 |
| 91668 | BAA10g01610 | A10 | 787856 | G | A | upstream_gene_variant | MODIFIER | c.-4436C>T| |
S66 |
| 91669 | BAA10g01620 | A10 | 788615 | C | T | upstream_gene_variant | MODIFIER | c.-3238G>A| |
S231 |
| 91670 | BAA10g01620 | A10 | 790195 | C | T | upstream_gene_variant | MODIFIER | c.-4818G>A| |
S139 |
| 91671 | BAA10g01630 | A10 | 790901 | G | A | downstream_gene_variant | MODIFIER | c.*2277C>T| |
S66 |
| 91672 | BAA10g01630 | A10 | 791668 | C | T | downstream_gene_variant | MODIFIER | c.*1510G>A| |
S104 S52 |
| 91673 | BAA10g01630 | A10 | 791736 | C | T | downstream_gene_variant | MODIFIER | c.*1442G>A| |
S275 |
| 91674 | BAA10g01630 | A10 | 792355 | G | A | downstream_gene_variant | MODIFIER | c.*823C>T| |
S276 |
| 91675 | BAA10g01630 | A10 | 793636 | C | T | missense_variant | MODERATE | c.439G>A|p.Gly147Arg |
S44 |