| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 136051 | BAA10g21750 | A10 | 19021202 | G | A | downstream_gene_variant | MODIFIER | c.*1292G>A| |
S236 |
| 136052 | BAA10g21750 | A10 | 19021387 | G | A | downstream_gene_variant | MODIFIER | c.*1477G>A| |
S271 |
| 136053 | BAA10g21760 | A10 | 19022177 | G | A | synonymous_variant | LOW | c.420C>T|p.His140His |
S1 S90 |
| 136054 | BAA10g21750 | A10 | 19022543 | G | A | downstream_gene_variant | MODIFIER | c.*2633G>A| |
S71 |
| 136055 | BAA10g21750 | A10 | 19022598 | C | T | downstream_gene_variant | MODIFIER | c.*2688C>T| |
S294 |
| 136056 | BAA10g21760 | A10 | 19023168 | C | T | upstream_gene_variant | MODIFIER | c.-73G>A| |
S296 |
| 136057 | BAA10g21760 | A10 | 19024438 | G | A | upstream_gene_variant | MODIFIER | c.-1343C>T| |
S15 |
| 136058 | BAA10g21760 | A10 | 19027437 | G | A | upstream_gene_variant | MODIFIER | c.-4342C>T| |
S136 |
| 136059 | BAA10g21770 | A10 | 19029504 | C | T | upstream_gene_variant | MODIFIER | c.-3442C>T| |
S189 S226 S250 |
| 136060 | BAA10g21770 | A10 | 19033787 | C | T | missense_variant | MODERATE | c.842C>T|p.Ala281Val |
S152 |
| 136061 | BAA10g21780 | A10 | 19037410 | C | T | synonymous_variant | LOW | c.570G>A|p.Gln190Gln |
S186 |
| 136062 | BAA10g21780 | A10 | 19037484 | G | A | missense_variant | MODERATE | c.496C>T|p.Pro166Ser |
S289 S290 |
| 136063 | BAA10g21780 | A10 | 19037549 | G | A | missense_variant | MODERATE | c.431C>T|p.Ser144Phe |
S82 S92 |
| 136064 | BAA10g21780 | A10 | 19037760 | G | A | missense_variant | MODERATE | c.308C>T|p.Thr103Met |
S149 |
| 136065 | BAA10g21780 | A10 | 19038789 | C | T | upstream_gene_variant | MODIFIER | c.-418G>A| |
S168 S219 |
| 136066 | BAA10g21780 | A10 | 19039232 | C | T | upstream_gene_variant | MODIFIER | c.-861G>A| |
S281 |
| 136067 | BAA10g21780 | A10 | 19040087 | C | T | upstream_gene_variant | MODIFIER | c.-1716G>A| |
S168 |
| 136068 | BAA10g21780 | A10 | 19040147 | C | T | upstream_gene_variant | MODIFIER | c.-1776G>A| |
S40 S49 |
| 136069 | BAA10g21780 | A10 | 19043194 | G | A | upstream_gene_variant | MODIFIER | c.-4823C>T| |
S203 |
| 136070 | BAA10g21790 | A10 | 19044372 | G | A | upstream_gene_variant | MODIFIER | c.-119C>T| |
S256 |
| 136071 | BAA10g21790 | A10 | 19044420 | G | A | upstream_gene_variant | MODIFIER | c.-167C>T| |
S131 |
| 136072 | BAA10g21800 | A10 | 19045282 | G | A | missense_variant | MODERATE | c.521G>A|p.Gly174Glu |
S182 |
| 136073 | BAA10g21800 | A10 | 19045401 | C | T | synonymous_variant | LOW | c.640C>T|p.Leu214Leu |
S148 S210 S30 S31 |
| 136074 | BAA10g21800 | A10 | 19045551 | G | A | missense_variant | MODERATE | c.790G>A|p.Gly264Arg |
S239 |
| 136075 | BAA10g21800 | A10 | 19045917 | G | A | missense_variant | MODERATE | c.1156G>A|p.Gly386Ser |
S195 |