| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 97201 | BAA10g05140 | A10 | 2664585 | C | T | downstream_gene_variant | MODIFIER | c.*1856C>T| |
S202 |
| 97202 | BAA10g05140 | A10 | 2664607 | C | T | downstream_gene_variant | MODIFIER | c.*1878C>T| |
S23 |
| 97203 | BAA10g05140 | A10 | 2664640 | G | A | downstream_gene_variant | MODIFIER | c.*1911G>A| |
S12 |
| 97204 | BAA10g05140 | A10 | 2664701 | G | A | downstream_gene_variant | MODIFIER | c.*1972G>A| |
S20 |
| 97205 | BAA10g05140 | A10 | 2664908 | G | A | downstream_gene_variant | MODIFIER | c.*2179G>A| |
S216 |
| 97206 | BAA10g05140 | A10 | 2665545 | G | A | downstream_gene_variant | MODIFIER | c.*2816G>A| |
S192 |
| 97207 | BAA10g05140 | A10 | 2666197 | C | T | downstream_gene_variant | MODIFIER | c.*3468C>T| |
S56 |
| 97208 | BAA10g05140 | A10 | 2666735 | C | T | downstream_gene_variant | MODIFIER | c.*4006C>T| |
S79 S91 |
| 97209 | BAA10g05140 | A10 | 2667569 | G | A | downstream_gene_variant | MODIFIER | c.*4840G>A| |
S157 S163 |
| 97210 | BAA10g05150 | A10 | 2668041 | G | A | downstream_gene_variant | MODIFIER | c.*2468C>T| |
S198 |
| 97211 | BAA10g05150 | A10 | 2668451 | G | A | downstream_gene_variant | MODIFIER | c.*2058C>T| |
S255 |
| 97212 | BAA10g05150 | A10 | 2669118 | G | A | downstream_gene_variant | MODIFIER | c.*1391C>T| |
S291 |
| 97213 | BAA10g05150 | A10 | 2669199 | G | A | downstream_gene_variant | MODIFIER | c.*1310C>T| |
S192 |
| 97214 | BAA10g05150 | A10 | 2669223 | G | A | downstream_gene_variant | MODIFIER | c.*1286C>T| |
S129 |
| 97215 | BAA10g05150 | A10 | 2669358 | G | A | downstream_gene_variant | MODIFIER | c.*1151C>T| |
S262 |
| 97216 | BAA10g05150 | A10 | 2669887 | C | T | downstream_gene_variant | MODIFIER | c.*622G>A| |
S188 |
| 97217 | BAA10g05150 | A10 | 2670133 | C | T | downstream_gene_variant | MODIFIER | c.*376G>A| |
S47 |
| 97218 | BAA10g05150 | A10 | 2670574 | C | T | missense_variant | MODERATE | c.694G>A|p.Gly232Arg |
S204 |
| 97219 | BAA10g05150 | A10 | 2670857 | C | T | missense_variant | MODERATE | c.505G>A|p.Gly169Ser |
S130 |
| 97220 | BAA10g05150 | A10 | 2671041 | G | A | intron_variant | MODIFIER | c.453+24C>T| |
S216 |
| 97221 | BAA10g05150 | A10 | 2671835 | C | T | stop_gained | HIGH | c.164G>A|p.Trp55* |
S70 |
| 97222 | BAA10g05150 | A10 | 2671980 | C | T | missense_variant | MODERATE | c.19G>A|p.Asp7Asn |
S34 |
| 97223 | BAA10g05150 | A10 | 2672991 | G | A | upstream_gene_variant | MODIFIER | c.-993C>T| |
S18 S92 |
| 97224 | BAA10g05150 | A10 | 2673201 | G | A | upstream_gene_variant | MODIFIER | c.-1203C>T| |
S283 |
| 97225 | BAA10g05150 | A10 | 2673272 | C | T | upstream_gene_variant | MODIFIER | c.-1274G>A| |
S152 |