| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123601 | BAA10g13490 | A10 | 14549470 | C | T | upstream_gene_variant | MODIFIER | c.-3883G>A| |
S202 |
| 123602 | BAA10g13500 | A10 | 14551924 | G | A | upstream_gene_variant | MODIFIER | c.-3272C>T| |
S234 |
| 123603 | BAA10g13500 | A10 | 14552041 | G | A | upstream_gene_variant | MODIFIER | c.-3389C>T| |
S64 |
| 123604 | BAA10g13500 | A10 | 14552299 | C | T | upstream_gene_variant | MODIFIER | c.-3647G>A| |
S249 |
| 123605 | BAA10g13510 | A10 | 14552691 | C | T | stop_gained | HIGH | c.2343G>A|p.Trp781* |
S5 |
| 123606 | BAA10g13510 | A10 | 14552957 | C | T | missense_variant | MODERATE | c.2077G>A|p.Glu693Lys |
S170 |
| 123607 | BAA10g13510 | A10 | 14554713 | G | A | synonymous_variant | LOW | c.321C>T|p.Ile107Ile |
S109 |
| 123608 | BAA10g13510 | A10 | 14554934 | C | T | missense_variant | MODERATE | c.100G>A|p.Val34Ile |
S87 |
| 123609 | BAA10g13540 | A10 | 14560101 | C | T | missense_variant | MODERATE | c.440G>A|p.Gly147Asp |
S244 |
| 123610 | BAA10g13520 | A10 | 14560671 | G | A | upstream_gene_variant | MODIFIER | c.-4608C>T| |
S116 S118 S148 S295 S30 S31 S54 |
| 123611 | BAA10g13520 | A10 | 14560922 | G | A | upstream_gene_variant | MODIFIER | c.-4859C>T| |
S212 |
| 123612 | BAA10g13550 | A10 | 14563077 | C | T | synonymous_variant | LOW | c.222C>T|p.Ile74Ile |
S298 |
| 123613 | BAA10g13550 | A10 | 14563886 | G | A | missense_variant | MODERATE | c.1031G>A|p.Arg344Lys |
S228 |
| 123614 | BAA10g13550 | A10 | 14563944 | G | A | synonymous_variant | LOW | c.1089G>A|p.Ala363Ala |
S13 |
| 123615 | BAA10g13550 | A10 | 14563976 | C | T | missense_variant | MODERATE | c.1121C>T|p.Ser374Leu |
S246 |
| 123616 | BAA10g13550 | A10 | 14564283 | G | A | synonymous_variant | LOW | c.1428G>A|p.Gln476Gln |
S80 |
| 123617 | BAA10g13550 | A10 | 14564372 | C | T | missense_variant | MODERATE | c.1517C>T|p.Thr506Ile |
S284 |
| 123618 | BAA10g13550 | A10 | 14564491 | G | A | missense_variant | MODERATE | c.1636G>A|p.Val546Met |
S62 |
| 123619 | BAA10g13550 | A10 | 14564703 | G | A | synonymous_variant | LOW | c.1848G>A|p.Glu616Glu |
S223 |
| 123620 | BAA10g13540 | A10 | 14565594 | G | A | upstream_gene_variant | MODIFIER | c.-4305C>T| |
S279 |
| 123621 | BAA10g13560 | A10 | 14566455 | C | T | upstream_gene_variant | MODIFIER | c.-1465C>T| |
S200 |
| 123622 | BAA10g13560 | A10 | 14567451 | C | T | upstream_gene_variant | MODIFIER | c.-469C>T| |
S188 |
| 123623 | BAA10g13550 | A10 | 14568134 | G | A | downstream_gene_variant | MODIFIER | c.*3281G>A| |
S1 S90 |
| 123624 | BAA10g13560 | A10 | 14568642 | G | A | synonymous_variant | LOW | c.630G>A|p.Lys210Lys |
S279 |
| 123625 | BAA10g13560 | A10 | 14569232 | C | T | missense_variant | MODERATE | c.1220C>T|p.Thr407Ile |
S225 S73 |