| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 149151 | BAA10g33310 | A10 | 23726405 | C | T | upstream_gene_variant | MODIFIER | c.-1888G>A| |
S47 |
| 149152 | BAA10g33310 | A10 | 23726837 | G | A | upstream_gene_variant | MODIFIER | c.-2320C>T| |
S164 |
| 149153 | BAA10g33310 | A10 | 23727025 | C | T | upstream_gene_variant | MODIFIER | c.-2508G>A| |
S63 |
| 149154 | BAA10g33320 | A10 | 23727296 | C | T | missense_variant | MODERATE | c.1390G>A|p.Asp464Asn |
S190 |
| 149155 | BAA10g33320 | A10 | 23727368 | C | T | missense_variant | MODERATE | c.1318G>A|p.Glu440Lys |
S69 |
| 149156 | BAA10g33320 | A10 | 23728340 | G | A | missense_variant | MODERATE | c.346C>T|p.His116Tyr |
S219 |
| 149157 | BAA10g33310 | A10 | 23728845 | C | T | upstream_gene_variant | MODIFIER | c.-4328G>A| |
S19 |
| 149158 | BAA10g33310 | A10 | 23729151 | C | T | upstream_gene_variant | MODIFIER | c.-4634G>A| |
S37 |
| 149159 | BAA10g33320 | A10 | 23730525 | G | A | upstream_gene_variant | MODIFIER | c.-1840C>T| |
S237 |
| 149160 | BAA10g33320 | A10 | 23731595 | C | T | upstream_gene_variant | MODIFIER | c.-2910G>A| |
S218 |
| 149161 | BAA10g33320 | A10 | 23732534 | G | A | upstream_gene_variant | MODIFIER | c.-3849C>T| |
S179 |
| 149162 | BAA10g33340 | A10 | 23733231 | G | A | missense_variant | MODERATE | c.908G>A|p.Gly303Glu |
S280 |
| 149163 | BAA10g33340 | A10 | 23733242 | G | A | missense_variant | MODERATE | c.919G>A|p.Glu307Lys |
S64 |
| 149164 | BAA10g33340 | A10 | 23734538 | G | A | missense_variant | MODERATE | c.2215G>A|p.Glu739Lys |
S252 |
| 149165 | BAA10g33340 | A10 | 23735021 | G | A | missense_variant | MODERATE | c.2698G>A|p.Asp900Asn |
S202 |
| 149166 | BAA10g33340 | A10 | 23736326 | G | A | missense_variant | MODERATE | c.4003G>A|p.Asp1335Asn |
S17 |
| 149167 | BAA10g33350 | A10 | 23742354 | G | A | synonymous_variant | LOW | c.78G>A|p.Glu26Glu |
S171 |
| 149168 | BAA10g33350 | A10 | 23742854 | G | A | missense_variant | MODERATE | c.578G>A|p.Arg193Lys |
S263 |
| 149169 | BAA10g33350 | A10 | 23743060 | C | T | synonymous_variant | LOW | c.784C>T|p.Leu262Leu |
S153 S213 |
| 149170 | BAA10g33360 | A10 | 23743331 | C | T | upstream_gene_variant | MODIFIER | c.-613C>T| |
S176 |
| 149171 | BAA10g33360 | A10 | 23743906 | C | T | upstream_gene_variant | MODIFIER | c.-38C>T| |
S10 S158 |
| 149172 | BAA10g33360 | A10 | 23743908 | C | T | upstream_gene_variant | MODIFIER | c.-36C>T| |
S224 |
| 149173 | BAA10g33360 | A10 | 23744408 | G | A | synonymous_variant | LOW | c.51G>A|p.Arg17Arg |
S128 S77 |
| 149174 | BAA10g33380 | A10 | 23746233 | G | A | upstream_gene_variant | MODIFIER | c.-2840G>A| |
S35 |
| 149175 | BAA10g33380 | A10 | 23749443 | C | T | missense_variant | MODERATE | c.371C>T|p.Ser124Phe |
S74 |