| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 97001 | BAA10g05060 | A10 | 2607982 | G | A | missense_variant | MODERATE | c.1312G>A|p.Gly438Arg |
S45 |
| 97002 | BAA10g05060 | A10 | 2608979 | G | A | missense_variant | MODERATE | c.2122G>A|p.Glu708Lys |
S211 S227 |
| 97003 | BAA10g05080 | A10 | 2609760 | C | T | upstream_gene_variant | MODIFIER | c.-3381C>T| |
S294 |
| 97004 | BAA10g05080 | A10 | 2610176 | G | A | upstream_gene_variant | MODIFIER | c.-2965G>A| |
S158 |
| 97005 | BAA10g05070 | A10 | 2610443 | G | A | synonymous_variant | LOW | c.961C>T|p.Leu321Leu |
S32 |
| 97006 | BAA10g05070 | A10 | 2611189 | G | A | synonymous_variant | LOW | c.288C>T|p.Ile96Ile |
S66 |
| 97007 | BAA10g05070 | A10 | 2611602 | C | T | upstream_gene_variant | MODIFIER | c.-50G>A| |
S232 |
| 97008 | BAA10g05070 | A10 | 2612002 | C | T | upstream_gene_variant | MODIFIER | c.-450G>A| |
S68 |
| 97009 | BAA10g05070 | A10 | 2612289 | G | A | upstream_gene_variant | MODIFIER | c.-737C>T| |
S157 S166 S167 S262 |
| 97010 | BAA10g05070 | A10 | 2613099 | C | T | upstream_gene_variant | MODIFIER | c.-1547G>A| |
S11 |
| 97011 | BAA10g05080 | A10 | 2613243 | C | T | missense_variant | MODERATE | c.103C>T|p.Pro35Ser |
S47 |
| 97012 | BAA10g05080 | A10 | 2613287 | C | T | synonymous_variant | LOW | c.147C>T|p.Tyr49Tyr |
S244 |
| 97013 | BAA10g05080 | A10 | 2613430 | C | T | missense_variant | MODERATE | c.290C>T|p.Ser97Phe |
S15 S156 S2 S3 S34 |
| 97014 | BAA10g05080 | A10 | 2613896 | G | A | missense_variant | MODERATE | c.674G>A|p.Cys225Tyr |
S303 |
| 97015 | BAA10g05080 | A10 | 2614153 | G | A | missense_variant | MODERATE | c.931G>A|p.Gly311Arg |
S125 S164 |
| 97016 | BAA10g05070 | A10 | 2615429 | C | T | upstream_gene_variant | MODIFIER | c.-3877G>A| |
S143 |
| 97017 | BAA10g05070 | A10 | 2615635 | G | A | upstream_gene_variant | MODIFIER | c.-4083C>T| |
S70 |
| 97018 | BAA10g05080 | A10 | 2616834 | G | A | downstream_gene_variant | MODIFIER | c.*2577G>A| |
S158 |
| 97019 | BAA10g05080 | A10 | 2616844 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S139 |
| 97020 | BAA10g05080 | A10 | 2617363 | C | T | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S203 |
| 97021 | BAA10g05090 | A10 | 2618676 | G | A | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S133 |
| 97022 | BAA10g05090 | A10 | 2619916 | G | A | upstream_gene_variant | MODIFIER | c.-1158C>T| |
S128 |
| 97023 | BAA10g05090 | A10 | 2619994 | G | A | upstream_gene_variant | MODIFIER | c.-1236C>T| |
S192 |
| 97024 | BAA10g05090 | A10 | 2620392 | G | A | upstream_gene_variant | MODIFIER | c.-1634C>T| |
S109 |
| 97025 | BAA10g05090 | A10 | 2620393 | C | T | upstream_gene_variant | MODIFIER | c.-1635G>A| |
S139 S205 |