| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 98001 | BAA10g05730 | A10 | 2944822 | C | T | synonymous_variant | LOW | c.1006C>T|p.Leu336Leu |
S10 |
| 98002 | BAA10g05730 | A10 | 2944838 | G | A | missense_variant | MODERATE | c.1022G>A|p.Gly341Asp |
S111 |
| 98003 | BAA10g05730 | A10 | 2944933 | G | A | missense_variant | MODERATE | c.1117G>A|p.Glu373Lys |
S172 S217 |
| 98004 | BAA10g05730 | A10 | 2945023 | G | A | missense_variant | MODERATE | c.1207G>A|p.Val403Met |
S12 |
| 98005 | BAA10g05730 | A10 | 2945078 | C | T | missense_variant | MODERATE | c.1262C>T|p.Pro421Leu |
S233 |
| 98006 | BAA10g05730 | A10 | 2945396 | C | T | missense_variant | MODERATE | c.1580C>T|p.Ser527Phe |
S35 |
| 98007 | BAA10g05730 | A10 | 2945457 | C | T | synonymous_variant | LOW | c.1641C>T|p.Ile547Ile |
S19 S305 S35 |
| 98008 | BAA10g05740 | A10 | 2945721 | C | T | upstream_gene_variant | MODIFIER | c.-89C>T| |
S132 S137 S215 S89 |
| 98009 | BAA10g05740 | A10 | 2946517 | C | T | synonymous_variant | LOW | c.708C>T|p.Asp236Asp |
S208 S93 |
| 98010 | BAA10g05730 | A10 | 2947146 | C | T | downstream_gene_variant | MODIFIER | c.*1575C>T| |
S302 |
| 98011 | BAA10g05730 | A10 | 2947214 | G | A | downstream_gene_variant | MODIFIER | c.*1643G>A| |
S45 |
| 98012 | BAA10g05730 | A10 | 2947766 | C | T | downstream_gene_variant | MODIFIER | c.*2195C>T| |
S260 |
| 98013 | BAA10g05730 | A10 | 2947782 | C | T | downstream_gene_variant | MODIFIER | c.*2211C>T| |
S169 |
| 98014 | BAA10g05730 | A10 | 2948234 | A | T | downstream_gene_variant | MODIFIER | c.*2663A>T| |
S69 |
| 98015 | BAA10g05730 | A10 | 2949032 | G | A | downstream_gene_variant | MODIFIER | c.*3461G>A| |
S151 S263 |
| 98016 | BAA10g05730 | A10 | 2949352 | C | T | downstream_gene_variant | MODIFIER | c.*3781C>T| |
S162 |
| 98017 | BAA10g05750 | A10 | 2950184 | G | A | upstream_gene_variant | MODIFIER | c.-4192G>A| |
S302 |
| 98018 | BAA10g05750 | A10 | 2951160 | C | T | upstream_gene_variant | MODIFIER | c.-3216C>T| |
S113 |
| 98019 | BAA10g05750 | A10 | 2953659 | C | T | upstream_gene_variant | MODIFIER | c.-717C>T| |
S115 |
| 98020 | BAA10g05750 | A10 | 2954512 | G | A | missense_variant | MODERATE | c.137G>A|p.Gly46Glu |
S212 |
| 98021 | BAA10g05750 | A10 | 2954771 | C | T | synonymous_variant | LOW | c.396C>T|p.Ala132Ala |
S297 |
| 98022 | BAA10g05770 | A10 | 2955084 | T | G | upstream_gene_variant | MODIFIER | c.-4570T>G| |
|
| 98023 | BAA10g05750 | A10 | 2955384 | G | A | missense_variant | MODERATE | c.760G>A|p.Ala254Thr |
S17 |
| 98024 | BAA10g05750 | A10 | 2955497 | G | A | synonymous_variant | LOW | c.873G>A|p.Lys291Lys |
S43 |
| 98025 | BAA10g05760 | A10 | 2957007 | G | A | missense_variant | MODERATE | c.772C>T|p.Arg258Cys |
S138 |