| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 129951 | BAA10g17710 | A10 | 16904187 | C | T | missense_variant | MODERATE | c.218C>T|p.Pro73Leu |
S103 |
| 129952 | BAA10g17680 | A10 | 16904770 | G | A | upstream_gene_variant | MODIFIER | c.-4138C>T| |
S239 |
| 129953 | BAA10g17710 | A10 | 16904825 | G | A | missense_variant | MODERATE | c.587G>A|p.Arg196His |
S174 S27 |
| 129954 | BAA10g17680 | A10 | 16905196 | G | A | upstream_gene_variant | MODIFIER | c.-4564C>T| |
S138 |
| 129955 | BAA10g17680 | A10 | 16905389 | C | T | upstream_gene_variant | MODIFIER | c.-4757G>A| |
S203 |
| 129956 | BAA10g17720 | A10 | 16905915 | G | A | missense_variant | MODERATE | c.920C>T|p.Pro307Leu |
S172 S217 |
| 129957 | BAA10g17720 | A10 | 16906523 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.608-1G>A| |
S125 |
| 129958 | BAA10g17730 | A10 | 16907467 | G | A | upstream_gene_variant | MODIFIER | c.-1372G>A| |
S42 |
| 129959 | BAA10g17720 | A10 | 16907563 | C | T | stop_gained | HIGH | c.318G>A|p.Trp106* |
S46 |
| 129960 | BAA10g17720 | A10 | 16908107 | C | T | synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S199 |
| 129961 | BAA10g17730 | A10 | 16909589 | G | A | missense_variant | MODERATE | c.598G>A|p.Val200Met |
S202 |
| 129962 | BAA10g17730 | A10 | 16910259 | C | T | missense_variant | MODERATE | c.1181C>T|p.Ser394Phe |
S142 |
| 129963 | BAA10g17730 | A10 | 16910321 | G | A | missense_variant | MODERATE | c.1243G>A|p.Val415Ile |
S43 |
| 129964 | BAA10g17730 | A10 | 16911106 | G | A | missense_variant | MODERATE | c.1853G>A|p.Arg618Lys |
S192 |
| 129965 | BAA10g17720 | A10 | 16911481 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S151 S263 |
| 129966 | BAA10g17720 | A10 | 16912199 | G | A | upstream_gene_variant | MODIFIER | c.-4021C>T| |
S178 |
| 129967 | BAA10g17730 | A10 | 16914005 | G | A | downstream_gene_variant | MODIFIER | c.*2877G>A| |
S221 |
| 129968 | BAA10g17730 | A10 | 16914155 | C | T | downstream_gene_variant | MODIFIER | c.*3027C>T| |
S281 |
| 129969 | BAA10g17730 | A10 | 16914857 | C | T | downstream_gene_variant | MODIFIER | c.*3729C>T| |
S117 |
| 129970 | BAA10g17740 | A10 | 16916080 | G | A | missense_variant | MODERATE | c.326C>T|p.Thr109Met |
S202 |
| 129971 | BAA10g17740 | A10 | 16916114 | T | C | missense_variant | MODERATE | c.292A>G|p.Ser98Gly |
S128 |
| 129972 | BAA10g17740 | A10 | 16917260 | C | T | upstream_gene_variant | MODIFIER | c.-855G>A| |
S25 |
| 129973 | BAA10g17740 | A10 | 16917509 | C | T | upstream_gene_variant | MODIFIER | c.-1104G>A| |
S153 S213 |
| 129974 | BAA10g17740 | A10 | 16918205 | C | T | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S259 |
| 129975 | BAA10g17740 | A10 | 16918382 | C | T | upstream_gene_variant | MODIFIER | c.-1977G>A| |
S308 |