| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 149051 | BAA10g33230 | A10 | 23697122 | G | A | upstream_gene_variant | MODIFIER | c.-4046C>T| |
S94 |
| 149052 | BAA10g33230 | A10 | 23697491 | G | A | upstream_gene_variant | MODIFIER | c.-4415C>T| |
S262 |
| 149053 | BAA10g33240 | A10 | 23698708 | C | T | upstream_gene_variant | MODIFIER | c.-2281G>A| |
S225 |
| 149054 | BAA10g33240 | A10 | 23698931 | G | A | upstream_gene_variant | MODIFIER | c.-2504C>T| |
S251 |
| 149055 | BAA10g33250 | A10 | 23699281 | G | A | stop_gained | HIGH | c.75G>A|p.Trp25* |
S276 |
| 149056 | BAA10g33250 | A10 | 23699385 | G | A | missense_variant | MODERATE | c.179G>A|p.Arg60Gln |
S192 |
| 149057 | BAA10g33250 | A10 | 23699408 | C | T | missense_variant | MODERATE | c.202C>T|p.Pro68Ser |
S296 |
| 149058 | BAA10g33240 | A10 | 23700640 | G | A | upstream_gene_variant | MODIFIER | c.-4213C>T| |
S262 |
| 149059 | BAA10g33240 | A10 | 23700929 | G | A | upstream_gene_variant | MODIFIER | c.-4502C>T| |
S223 |
| 149060 | BAA10g33260 | A10 | 23701661 | C | T | upstream_gene_variant | MODIFIER | c.-3232C>T| |
S104 |
| 149061 | BAA10g33260 | A10 | 23701846 | G | A | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S1 S219 S72 |
| 149062 | BAA10g33260 | A10 | 23701951 | C | T | upstream_gene_variant | MODIFIER | c.-2942C>T| |
S142 |
| 149063 | BAA10g33260 | A10 | 23702690 | C | T | upstream_gene_variant | MODIFIER | c.-2203C>T| |
S83 S88 |
| 149064 | BAA10g33250 | A10 | 23703807 | C | T | splice_region_variant&intron_variant | LOW | c.703-7C>T| |
S301 S304 |
| 149065 | BAA10g33250 | A10 | 23704028 | G | A | missense_variant | MODERATE | c.835G>A|p.Ala279Thr |
S173 |
| 149066 | BAA10g33260 | A10 | 23704868 | C | T | upstream_gene_variant | MODIFIER | c.-25C>T| |
S206 S26 |
| 149067 | BAA10g33260 | A10 | 23704876 | C | T | upstream_gene_variant | MODIFIER | c.-17C>T| |
S169 |
| 149068 | BAA10g33260 | A10 | 23705351 | G | A | synonymous_variant | LOW | c.459G>A|p.Gly153Gly |
S1 S90 |
| 149069 | BAA10g33250 | A10 | 23705779 | G | A | downstream_gene_variant | MODIFIER | c.*1103G>A| |
S132 S137 S215 |
| 149070 | BAA10g33250 | A10 | 23706829 | C | T | downstream_gene_variant | MODIFIER | c.*2153C>T| |
S18 |
| 149071 | BAA10g33250 | A10 | 23707787 | C | T | downstream_gene_variant | MODIFIER | c.*3111C>T| |
S283 |
| 149072 | BAA10g33270 | A10 | 23709254 | G | A | upstream_gene_variant | MODIFIER | c.-78C>T| |
S54 |
| 149073 | BAA10g33280 | A10 | 23710582 | G | A | splice_region_variant&intron_variant | LOW | c.809+6C>T| |
S259 |
| 149074 | BAA10g33280 | A10 | 23711238 | G | A | synonymous_variant | LOW | c.409C>T|p.Leu137Leu |
S217 S248 |
| 149075 | BAA10g33280 | A10 | 23711806 | G | A | missense_variant | MODERATE | c.155C>T|p.Ser52Phe |
S265 |