| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 151051 | BAA10g34940 | A10 | 24424450 | C | T | downstream_gene_variant | MODIFIER | c.*4137C>T| |
S186 |
| 151052 | BAA10g34940 | A10 | 24424756 | G | A | downstream_gene_variant | MODIFIER | c.*4443G>A| |
S172 S217 |
| 151053 | BAA10g34940 | A10 | 24425203 | G | A | downstream_gene_variant | MODIFIER | c.*4890G>A| |
S95 |
| 151054 | BAA10g34950 | A10 | 24426656 | G | A | downstream_gene_variant | MODIFIER | c.*3240G>A| |
S100 |
| 151055 | BAA10g34960 | A10 | 24426729 | C | T | synonymous_variant | LOW | c.1350G>A|p.Glu450Glu |
S152 |
| 151056 | BAA10g34950 | A10 | 24427831 | C | T | downstream_gene_variant | MODIFIER | c.*4415C>T| |
S97 |
| 151057 | BAA10g34960 | A10 | 24430146 | C | T | upstream_gene_variant | MODIFIER | c.-1282G>A| |
S186 |
| 151058 | BAA10g34960 | A10 | 24430200 | G | A | upstream_gene_variant | MODIFIER | c.-1336C>T| |
S99 |
| 151059 | BAA10g34960 | A10 | 24431317 | G | A | upstream_gene_variant | MODIFIER | c.-2453C>T| |
S293 |
| 151060 | BAA10g34970 | A10 | 24431710 | G | A | missense_variant | MODERATE | c.317C>T|p.Ser106Leu |
S94 |
| 151061 | BAA10g34970 | A10 | 24432109 | C | T | missense_variant | MODERATE | c.5G>A|p.Gly2Glu |
S140 |
| 151062 | BAA10g34960 | A10 | 24432675 | C | T | upstream_gene_variant | MODIFIER | c.-3811G>A| |
S292 |
| 151063 | BAA10g34960 | A10 | 24432828 | G | A | upstream_gene_variant | MODIFIER | c.-3964C>T| |
S175 |
| 151064 | BAA10g34960 | A10 | 24433008 | G | A | upstream_gene_variant | MODIFIER | c.-4144C>T| |
S153 S213 |
| 151065 | BAA10g34960 | A10 | 24433500 | C | T | upstream_gene_variant | MODIFIER | c.-4636G>A| |
S177 |
| 151066 | BAA10g34960 | A10 | 24433774 | C | T | upstream_gene_variant | MODIFIER | c.-4910G>A| |
S67 |
| 151067 | BAA10g34980 | A10 | 24434514 | G | A | synonymous_variant | LOW | c.306G>A|p.Gly102Gly |
S28 |
| 151068 | BAA10g34990 | A10 | 24435563 | G | A | missense_variant | MODERATE | c.424C>T|p.Leu142Phe |
S172 S217 |
| 151069 | BAA10g34990 | A10 | 24436166 | C | T | splice_region_variant&intron_variant | LOW | c.112-5G>A| |
S153 S213 |
| 151070 | BAA10g34990 | A10 | 24436543 | C | T | missense_variant | MODERATE | c.68G>A|p.Cys23Tyr |
S146 |
| 151071 | BAA10g35000 | A10 | 24437368 | G | A | missense_variant | MODERATE | c.193G>A|p.Glu65Lys |
S178 |
| 151072 | BAA10g35000 | A10 | 24437451 | C | T | synonymous_variant | LOW | c.276C>T|p.Ser92Ser |
S308 |
| 151073 | BAA10g34990 | A10 | 24437954 | G | A | upstream_gene_variant | MODIFIER | c.-1237C>T| |
S16 |
| 151074 | BAA10g34990 | A10 | 24438219 | G | A | upstream_gene_variant | MODIFIER | c.-1502C>T| |
S127 S250 |
| 151075 | BAA10g34990 | A10 | 24438240 | G | A | upstream_gene_variant | MODIFIER | c.-1523C>T| |
S150 |