| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145201 | BAA10g29820 | A10 | 22298813 | G | A | missense_variant | MODERATE | c.445G>A|p.Glu149Lys |
S70 |
| 145202 | BAA10g29820 | A10 | 22299307 | G | A | missense_variant | MODERATE | c.709G>A|p.Glu237Lys |
S241 |
| 145203 | BAA10g29840 | A10 | 22300264 | G | A | upstream_gene_variant | MODIFIER | c.-4791G>A| |
S64 |
| 145204 | BAA10g29820 | A10 | 22300613 | G | A | missense_variant | MODERATE | c.1016G>A|p.Gly339Glu |
S9 |
| 145205 | BAA10g29820 | A10 | 22301009 | G | A | synonymous_variant | LOW | c.1245G>A|p.Leu415Leu |
S18 |
| 145206 | BAA10g29830 | A10 | 22302258 | G | A | missense_variant | MODERATE | c.1669C>T|p.Pro557Ser |
S228 |
| 145207 | BAA10g29830 | A10 | 22302537 | G | A | missense_variant | MODERATE | c.1390C>T|p.Pro464Ser |
S69 |
| 145208 | BAA10g29830 | A10 | 22302725 | G | A | missense_variant | MODERATE | c.1202C>T|p.Ser401Leu |
S308 |
| 145209 | BAA10g29830 | A10 | 22302780 | G | A | missense_variant | MODERATE | c.1147C>T|p.Pro383Ser |
S289 S290 |
| 145210 | BAA10g29830 | A10 | 22302933 | C | T | missense_variant | MODERATE | c.994G>A|p.Glu332Lys |
S247 |
| 145211 | BAA10g29830 | A10 | 22303151 | G | A | missense_variant | MODERATE | c.869C>T|p.Pro290Leu |
S59 |
| 145212 | BAA10g29830 | A10 | 22303746 | C | T | synonymous_variant | LOW | c.357G>A|p.Gln119Gln |
S72 |
| 145213 | BAA10g29830 | A10 | 22304725 | C | T | upstream_gene_variant | MODIFIER | c.-623G>A| |
S36 |
| 145214 | BAA10g29840 | A10 | 22305088 | C | T | missense_variant | MODERATE | c.34C>T|p.Pro12Ser |
S140 |
| 145215 | BAA10g29840 | A10 | 22306259 | C | T | missense_variant | MODERATE | c.856C>T|p.Leu286Phe |
S201 |
| 145216 | BAA10g29830 | A10 | 22306559 | C | T | upstream_gene_variant | MODIFIER | c.-2457G>A| |
S201 |
| 145217 | BAA10g29830 | A10 | 22307556 | G | A | upstream_gene_variant | MODIFIER | c.-3454C>T| |
S270 |
| 145218 | BAA10g29850 | A10 | 22308423 | C | T | splice_region_variant&synonymous_variant | LOW | c.3267G>A|p.Arg1089Arg |
S6 |
| 145219 | BAA10g29850 | A10 | 22308452 | C | T | missense_variant | MODERATE | c.3238G>A|p.Gly1080Arg |
S92 |
| 145220 | BAA10g29850 | A10 | 22309357 | C | T | missense_variant | MODERATE | c.2885G>A|p.Arg962Lys |
S135 |
| 145221 | BAA10g29850 | A10 | 22309571 | C | T | missense_variant | MODERATE | c.2819G>A|p.Gly940Glu |
S225 S73 |
| 145222 | BAA10g29850 | A10 | 22309811 | G | A | missense_variant | MODERATE | c.2675C>T|p.Pro892Leu |
S160 |
| 145223 | BAA10g29840 | A10 | 22310036 | C | T | downstream_gene_variant | MODIFIER | c.*3583C>T| |
S2 |
| 145224 | BAA10g29850 | A10 | 22310118 | G | A | splice_region_variant&intron_variant | LOW | c.2562+8C>T| |
S284 |
| 145225 | BAA10g29840 | A10 | 22310486 | C | T | downstream_gene_variant | MODIFIER | c.*4033C>T| |
S10 |