| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145051 | BAA10g29670 | A10 | 22248777 | C | T | upstream_gene_variant | MODIFIER | c.-4478G>A| |
S287 |
| 145052 | BAA10g29690 | A10 | 22249432 | C | T | missense_variant | MODERATE | c.992C>T|p.Thr331Met |
S135 |
| 145053 | BAA10g29680 | A10 | 22250346 | G | A | upstream_gene_variant | MODIFIER | c.-3504C>T| |
S132 S137 S215 S89 |
| 145054 | BAA10g29680 | A10 | 22250422 | C | T | upstream_gene_variant | MODIFIER | c.-3580G>A| |
S11 |
| 145055 | BAA10g29700 | A10 | 22252032 | G | A | missense_variant | MODERATE | c.1469C>T|p.Ser490Phe |
S240 |
| 145056 | BAA10g29700 | A10 | 22252642 | C | T | missense_variant | MODERATE | c.859G>A|p.Asp287Asn |
S260 |
| 145057 | BAA10g29700 | A10 | 22252657 | G | A | splice_region_variant&intron_variant | LOW | c.850-6C>T| |
S69 |
| 145058 | BAA10g29700 | A10 | 22252847 | C | T | synonymous_variant | LOW | c.729G>A|p.Lys243Lys |
S40 S49 |
| 145059 | BAA10g29700 | A10 | 22253429 | C | T | synonymous_variant | LOW | c.222G>A|p.Glu74Glu |
S299 |
| 145060 | BAA10g29700 | A10 | 22253540 | C | T | synonymous_variant | LOW | c.111G>A|p.Lys37Lys |
S157 S163 |
| 145061 | BAA10g29700 | A10 | 22253899 | C | T | upstream_gene_variant | MODIFIER | c.-249G>A| |
S14 |
| 145062 | BAA10g29700 | A10 | 22253919 | G | A | upstream_gene_variant | MODIFIER | c.-269C>T| |
S274 |
| 145063 | BAA10g29700 | A10 | 22256237 | G | A | upstream_gene_variant | MODIFIER | c.-2587C>T| |
S150 |
| 145064 | BAA10g29700 | A10 | 22256953 | C | T | upstream_gene_variant | MODIFIER | c.-3303G>A| |
S116 |
| 145065 | BAA10g29700 | A10 | 22257266 | C | T | upstream_gene_variant | MODIFIER | c.-3616G>A| |
S108 |
| 145066 | BAA10g29700 | A10 | 22257480 | G | A | upstream_gene_variant | MODIFIER | c.-3830C>T| |
S303 |
| 145067 | BAA10g29700 | A10 | 22257655 | G | A | upstream_gene_variant | MODIFIER | c.-4005C>T| |
S18 |
| 145068 | BAA10g29720 | A10 | 22258099 | G | A | missense_variant | MODERATE | c.350C>T|p.Thr117Ile |
S278 |
| 145069 | BAA10g29700 | A10 | 22258179 | G | A | upstream_gene_variant | MODIFIER | c.-4529C>T| |
S209 |
| 145070 | BAA10g29710 | A10 | 22260178 | G | T | upstream_gene_variant | MODIFIER | c.-3278C>A| |
S136 S275 |
| 145071 | BAA10g29710 | A10 | 22260422 | C | T | upstream_gene_variant | MODIFIER | c.-3522G>A| |
S235 |
| 145072 | BAA10g29710 | A10 | 22260534 | G | A | upstream_gene_variant | MODIFIER | c.-3634C>T| |
S118 |
| 145073 | BAA10g29710 | A10 | 22260615 | G | A | upstream_gene_variant | MODIFIER | c.-3715C>T| |
S199 |
| 145074 | BAA10g29730 | A10 | 22261251 | G | A | missense_variant | MODERATE | c.13G>A|p.Ala5Thr |
S71 |
| 145075 | BAA10g29730 | A10 | 22261610 | C | T | missense_variant | MODERATE | c.205C>T|p.Leu69Phe |
S281 |