| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 144301 | BAA10g28950 | A10 | 21996274 | C | T | upstream_gene_variant | MODIFIER | c.-3235G>A| |
S260 |
| 144302 | BAA10g28950 | A10 | 21996406 | C | T | upstream_gene_variant | MODIFIER | c.-3367G>A| |
S156 |
| 144303 | BAA10g28950 | A10 | 21996463 | C | T | upstream_gene_variant | MODIFIER | c.-3424G>A| |
S83 S88 |
| 144304 | BAA10g28950 | A10 | 21996804 | C | T | upstream_gene_variant | MODIFIER | c.-3765G>A| |
S2 |
| 144305 | BAA10g28950 | A10 | 21997242 | G | A | upstream_gene_variant | MODIFIER | c.-4203C>T| |
S164 |
| 144306 | BAA10g28970 | A10 | 21999379 | C | A | synonymous_variant | LOW | c.1251C>A|p.Leu417Leu |
S157 S163 |
| 144307 | BAA10g28970 | A10 | 21999470 | C | T | missense_variant | MODERATE | c.1342C>T|p.Pro448Ser |
S281 |
| 144308 | BAA10g28980 | A10 | 22000324 | C | T | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S189 |
| 144309 | BAA10g28980 | A10 | 22001612 | C | T | upstream_gene_variant | MODIFIER | c.-599C>T| |
S291 |
| 144310 | BAA10g28980 | A10 | 22001711 | G | A | upstream_gene_variant | MODIFIER | c.-500G>A| |
S62 |
| 144311 | BAA10g28980 | A10 | 22001836 | C | T | upstream_gene_variant | MODIFIER | c.-375C>T| |
S277 |
| 144312 | BAA10g28980 | A10 | 22002494 | C | T | synonymous_variant | LOW | c.201C>T|p.Phe67Phe |
S221 |
| 144313 | BAA10g29000 | A10 | 22006557 | G | A | upstream_gene_variant | MODIFIER | c.-107G>A| |
S139 |
| 144314 | BAA10g29010 | A10 | 22008427 | C | T | missense_variant | MODERATE | c.67C>T|p.Pro23Ser |
S56 |
| 144315 | BAA10g29020 | A10 | 22009607 | G | A | missense_variant | MODERATE | c.91G>A|p.Asp31Asn |
S16 |
| 144316 | BAA10g29020 | A10 | 22009763 | C | T | missense_variant | MODERATE | c.247C>T|p.Pro83Ser |
S54 |
| 144317 | BAA10g29050 | A10 | 22010945 | G | A | upstream_gene_variant | MODIFIER | c.-3380G>A| |
S240 |
| 144318 | BAA10g29030 | A10 | 22012272 | G | A | upstream_gene_variant | MODIFIER | c.-833C>T| |
S125 |
| 144319 | BAA10g29040 | A10 | 22013386 | C | T | missense_variant | MODERATE | c.223G>A|p.Val75Met |
S255 |
| 144320 | BAA10g29040 | A10 | 22013399 | G | A | synonymous_variant | LOW | c.210C>T|p.Asp70Asp |
S207 |
| 144321 | BAA10g29050 | A10 | 22014612 | G | A | stop_gained | HIGH | c.159G>A|p.Trp53* |
S76 |
| 144322 | BAA10g29030 | A10 | 22015358 | C | T | upstream_gene_variant | MODIFIER | c.-3919G>A| |
S20 |
| 144323 | BAA10g29030 | A10 | 22015446 | G | A | upstream_gene_variant | MODIFIER | c.-4007C>T| |
S279 |
| 144324 | BAA10g29030 | A10 | 22015770 | C | T | upstream_gene_variant | MODIFIER | c.-4331G>A| |
S130 |
| 144325 | BAA10g29040 | A10 | 22016511 | G | A | upstream_gene_variant | MODIFIER | c.-2599C>T| |
S192 |