| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 137051 | BAA10g22740 | A10 | 19417843 | G | A | upstream_gene_variant | MODIFIER | c.-4440C>T| |
S55 |
| 137052 | BAA10g22760 | A10 | 19417959 | G | A | missense_variant | MODERATE | c.154G>A|p.Gly52Ser |
S178 S50 |
| 137053 | BAA10g22760 | A10 | 19418148 | G | A | missense_variant | MODERATE | c.343G>A|p.Asp115Asn |
S32 |
| 137054 | BAA10g22760 | A10 | 19418648 | C | T | synonymous_variant | LOW | c.688C>T|p.Leu230Leu |
S196 |
| 137055 | BAA10g22750 | A10 | 19419107 | C | T | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S70 |
| 137056 | BAA10g22770 | A10 | 19419779 | G | A | missense_variant | MODERATE | c.259G>A|p.Glu87Lys |
S132 S137 S215 S89 |
| 137057 | BAA10g22770 | A10 | 19420228 | G | A | synonymous_variant | LOW | c.633G>A|p.Leu211Leu |
S15 S3 |
| 137058 | BAA10g22750 | A10 | 19420309 | G | A | upstream_gene_variant | MODIFIER | c.-3557C>T| |
S180 |
| 137059 | BAA10g22750 | A10 | 19420376 | C | T | upstream_gene_variant | MODIFIER | c.-3624G>A| |
S308 |
| 137060 | BAA10g22750 | A10 | 19420385 | G | A | upstream_gene_variant | MODIFIER | c.-3633C>T| |
S75 S81 |
| 137061 | BAA10g22760 | A10 | 19422662 | G | A | downstream_gene_variant | MODIFIER | c.*3875G>A| |
S62 |
| 137062 | BAA10g22760 | A10 | 19422706 | C | T | downstream_gene_variant | MODIFIER | c.*3919C>T| |
S229 |
| 137063 | BAA10g22790 | A10 | 19426205 | C | T | missense_variant | MODERATE | c.761G>A|p.Ser254Asn |
S107 |
| 137064 | BAA10g22790 | A10 | 19427838 | G | A | upstream_gene_variant | MODIFIER | c.-240C>T| |
S74 |
| 137065 | BAA10g22790 | A10 | 19427979 | G | A | upstream_gene_variant | MODIFIER | c.-381C>T| |
S251 |
| 137066 | BAA10g22790 | A10 | 19428014 | C | T | upstream_gene_variant | MODIFIER | c.-416G>A| |
S139 S306 S308 |
| 137067 | BAA10g22800 | A10 | 19429137 | G | A | missense_variant | MODERATE | c.34G>A|p.Asp12Asn |
S130 |
| 137068 | BAA10g22800 | A10 | 19429318 | C | T | missense_variant | MODERATE | c.215C>T|p.Ser72Phe |
S203 |
| 137069 | BAA10g22800 | A10 | 19429660 | C | T | missense_variant | MODERATE | c.557C>T|p.Ala186Val |
S186 |
| 137070 | BAA10g22800 | A10 | 19429896 | C | T | missense_variant | MODERATE | c.793C>T|p.Leu265Phe |
S73 |
| 137071 | BAA10g22800 | A10 | 19430339 | G | A | synonymous_variant | LOW | c.1236G>A|p.Glu412Glu |
S228 |
| 137072 | BAA10g22800 | A10 | 19430370 | G | A | missense_variant | MODERATE | c.1267G>A|p.Val423Met |
S9 |
| 137073 | BAA10g22790 | A10 | 19431085 | C | T | upstream_gene_variant | MODIFIER | c.-3487G>A| |
S282 |
| 137074 | BAA10g22810 | A10 | 19432865 | C | T | upstream_gene_variant | MODIFIER | c.-2224C>T| |
S135 |
| 137075 | BAA10g22810 | A10 | 19433345 | G | A | upstream_gene_variant | MODIFIER | c.-1744G>A| |
S69 |