| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 137301 | BAA10g22940 | A10 | 19513840 | G | A | upstream_gene_variant | MODIFIER | c.-2756G>A| |
S208 S219 |
| 137302 | BAA10g22940 | A10 | 19514024 | G | A | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S15 |
| 137303 | BAA10g22940 | A10 | 19515794 | C | T | upstream_gene_variant | MODIFIER | c.-802C>T| |
S86 |
| 137304 | BAA10g22940 | A10 | 19515801 | G | A | upstream_gene_variant | MODIFIER | c.-795G>A| |
S138 |
| 137305 | BAA10g22940 | A10 | 19516411 | C | T | upstream_gene_variant | MODIFIER | c.-185C>T| |
S10 |
| 137306 | BAA10g22940 | A10 | 19517041 | C | T | missense_variant | MODERATE | c.446C>T|p.Pro149Leu |
S96 |
| 137307 | BAA10g22940 | A10 | 19519507 | G | A | downstream_gene_variant | MODIFIER | c.*2339G>A| |
S9 |
| 137308 | BAA10g22940 | A10 | 19520342 | G | A | downstream_gene_variant | MODIFIER | c.*3174G>A| |
S216 |
| 137309 | BAA10g22940 | A10 | 19521517 | C | T | downstream_gene_variant | MODIFIER | c.*4349C>T| |
S39 |
| 137310 | BAA10g22940 | A10 | 19521907 | C | T | downstream_gene_variant | MODIFIER | c.*4739C>T| |
S262 |
| 137311 | BAA10g22940 | A10 | 19521941 | C | T | downstream_gene_variant | MODIFIER | c.*4773C>T| |
S11 |
| 137312 | BAA10g22950 | A10 | 19522684 | C | T | intron_variant | MODIFIER | c.292-512G>A| |
S23 |
| 137313 | BAA10g22950 | A10 | 19522770 | G | A | intron_variant | MODIFIER | c.292-598C>T| |
S161 |
| 137314 | BAA10g22950 | A10 | 19526413 | G | A | missense_variant | MODERATE | c.236C>T|p.Ser79Phe |
S136 |
| 137315 | BAA10g22950 | A10 | 19528523 | G | A | upstream_gene_variant | MODIFIER | c.-1791C>T| |
S16 |
| 137316 | BAA10g22950 | A10 | 19529867 | G | A | upstream_gene_variant | MODIFIER | c.-3135C>T| |
S15 S3 |
| 137317 | BAA10g22950 | A10 | 19530702 | C | A | upstream_gene_variant | MODIFIER | c.-3970G>T| |
S215 |
| 137318 | BAA10g22970 | A10 | 19535106 | G | A | upstream_gene_variant | MODIFIER | c.-4246G>A| |
S139 |
| 137319 | BAA10g22970 | A10 | 19538507 | C | T | upstream_gene_variant | MODIFIER | c.-845C>T| |
S146 |
| 137320 | BAA10g22970 | A10 | 19540158 | A | C | synonymous_variant | LOW | c.421A>C|p.Arg141Arg |
S133 S291 S297 |
| 137321 | BAA10g22970 | A10 | 19541173 | G | A | intron_variant | MODIFIER | c.942+133G>A| |
S166 |
| 137322 | BAA10g22980 | A10 | 19544269 | G | A | upstream_gene_variant | MODIFIER | c.-4813G>A| |
S212 |
| 137323 | BAA10g22980 | A10 | 19546505 | G | A | upstream_gene_variant | MODIFIER | c.-2577G>A| |
S271 |
| 137324 | BAA10g22980 | A10 | 19547505 | G | A | upstream_gene_variant | MODIFIER | c.-1577G>A| |
S118 |
| 137325 | BAA10g22980 | A10 | 19548498 | G | A | upstream_gene_variant | MODIFIER | c.-584G>A| |
S15 S3 |