| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 121601 | BAA10g12360-BAA10g12370 | A10 | 13820009 | G | A | intergenic_region | MODIFIER | n.13820009G>A| |
S198 |
| 121602 | BAA10g12370 | A10 | 13820621 | C | T | downstream_gene_variant | MODIFIER | c.*4589G>A| |
S135 |
| 121603 | BAA10g12370 | A10 | 13820938 | C | T | downstream_gene_variant | MODIFIER | c.*4272G>A| |
S193 |
| 121604 | BAA10g12370 | A10 | 13820994 | T | A | downstream_gene_variant | MODIFIER | c.*4216A>T| |
S84 S93 |
| 121605 | BAA10g12370 | A10 | 13821710 | G | A | downstream_gene_variant | MODIFIER | c.*3500C>T| |
S295 |
| 121606 | BAA10g12380 | A10 | 13824225 | C | T | upstream_gene_variant | MODIFIER | c.-3495C>T| |
S188 |
| 121607 | BAA10g12370 | A10 | 13825380 | G | A | upstream_gene_variant | MODIFIER | c.-9C>T| |
S290 |
| 121608 | BAA10g12370 | A10 | 13827313 | C | T | upstream_gene_variant | MODIFIER | c.-1942G>A| |
S183 |
| 121609 | BAA10g12380 | A10 | 13827729 | C | T | missense_variant | MODERATE | c.10C>T|p.Leu4Phe |
S187 |
| 121610 | BAA10g12380 | A10 | 13827989 | C | T | synonymous_variant | LOW | c.270C>T|p.Val90Val |
S176 |
| 121611 | BAA10g12370 | A10 | 13828759 | A | T | upstream_gene_variant | MODIFIER | c.-3388T>A| |
S112 |
| 121612 | BAA10g12370 | A10 | 13829237 | C | T | upstream_gene_variant | MODIFIER | c.-3866G>A| |
S115 |
| 121613 | BAA10g12370 | A10 | 13829473 | C | T | upstream_gene_variant | MODIFIER | c.-4102G>A| |
S276 |
| 121614 | BAA10g12370 | A10 | 13830152 | C | T | upstream_gene_variant | MODIFIER | c.-4781G>A| |
S301 S304 |
| 121615 | BAA10g12380 | A10 | 13832947 | C | T | downstream_gene_variant | MODIFIER | c.*2896C>T| |
S63 |
| 121616 | BAA10g12390 | A10 | 13833467 | C | T | missense_variant | MODERATE | c.830C>T|p.Ala277Val |
S19 |
| 121617 | BAA10g12400 | A10 | 13834851 | G | A | synonymous_variant | LOW | c.1051C>T|p.Leu351Leu |
S202 |
| 121618 | BAA10g12400 | A10 | 13835575 | C | T | splice_region_variant&intron_variant | LOW | c.501-8G>A| |
S199 |
| 121619 | BAA10g12400 | A10 | 13837723 | C | T | upstream_gene_variant | MODIFIER | c.-1161G>A| |
S190 |
| 121620 | BAA10g12400 | A10 | 13837834 | G | A | upstream_gene_variant | MODIFIER | c.-1272C>T| |
S100 |
| 121621 | BAA10g12400 | A10 | 13839068 | C | T | upstream_gene_variant | MODIFIER | c.-2506G>A| |
S17 |
| 121622 | BAA10g12400 | A10 | 13839877 | G | A | upstream_gene_variant | MODIFIER | c.-3315C>T| |
S288 |
| 121623 | BAA10g12400 | A10 | 13840450 | G | A | upstream_gene_variant | MODIFIER | c.-3888C>T| |
S151 S263 |
| 121624 | BAA10g12400 | A10 | 13840608 | C | T | upstream_gene_variant | MODIFIER | c.-4046G>A| |
S284 |
| 121625 | BAA10g12400 | A10 | 13840859 | G | A | upstream_gene_variant | MODIFIER | c.-4297C>T| |
S234 |