| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 121001 | BAA10g12160 | A10 | 13629372 | C | T | upstream_gene_variant | MODIFIER | c.-300G>A| |
S164 |
| 121002 | BAA10g12170 | A10 | 13629917 | C | T | missense_variant | MODERATE | c.2285G>A|p.Arg762Lys |
S196 |
| 121003 | BAA10g12170 | A10 | 13630014 | C | T | missense_variant | MODERATE | c.2188G>A|p.Gly730Ser |
S203 |
| 121004 | BAA10g12160 | A10 | 13631279 | C | T | upstream_gene_variant | MODIFIER | c.-2207G>A| |
S168 |
| 121005 | BAA10g12170 | A10 | 13632226 | G | A | synonymous_variant | LOW | c.837C>T|p.Asn279Asn |
S271 |
| 121006 | BAA10g12170 | A10 | 13632912 | C | T | missense_variant | MODERATE | c.151G>A|p.Asp51Asn |
S20 |
| 121007 | BAA10g12170 | A10 | 13632942 | C | T | missense_variant | MODERATE | c.121G>A|p.Asp41Asn |
S282 |
| 121008 | BAA10g12170 | A10 | 13632950 | G | A | missense_variant | MODERATE | c.113C>T|p.Ser38Phe |
S202 |
| 121009 | BAA10g12160 | A10 | 13633542 | G | A | upstream_gene_variant | MODIFIER | c.-4470C>T| |
S88 |
| 121010 | BAA10g12160 | A10 | 13633884 | C | T | upstream_gene_variant | MODIFIER | c.-4812G>A| |
S177 |
| 121011 | BAA10g12170 | A10 | 13634297 | C | T | upstream_gene_variant | MODIFIER | c.-1235G>A| |
S210 S225 |
| 121012 | BAA10g12170 | A10 | 13635999 | C | T | upstream_gene_variant | MODIFIER | c.-2937G>A| |
S190 |
| 121013 | BAA10g12170 | A10 | 13636022 | G | A | upstream_gene_variant | MODIFIER | c.-2960C>T| |
S151 S257 S263 |
| 121014 | BAA10g12170 | A10 | 13637043 | C | T | upstream_gene_variant | MODIFIER | c.-3981G>A| |
S305 |
| 121015 | BAA10g12170 | A10 | 13637511 | G | A | upstream_gene_variant | MODIFIER | c.-4449C>T| |
S228 |
| 121016 | BAA10g12170 | A10 | 13637752 | G | A | upstream_gene_variant | MODIFIER | c.-4690C>T| |
S171 |
| 121017 | BAA10g12170 | A10 | 13637958 | G | A | upstream_gene_variant | MODIFIER | c.-4896C>T| |
S192 |
| 121018 | BAA10g12180 | A10 | 13638067 | G | A | downstream_gene_variant | MODIFIER | c.*2677C>T| |
S13 S198 |
| 121019 | BAA10g12180 | A10 | 13639600 | G | A | downstream_gene_variant | MODIFIER | c.*1144C>T| |
S130 |
| 121020 | BAA10g12190 | A10 | 13641187 | G | A | downstream_gene_variant | MODIFIER | c.*1636C>T| |
S202 |
| 121021 | BAA10g12190 | A10 | 13641239 | C | T | downstream_gene_variant | MODIFIER | c.*1584G>A| |
S84 S93 |
| 121022 | BAA10g12180 | A10 | 13641973 | G | A | missense_variant | MODERATE | c.167C>T|p.Pro56Leu |
S192 |
| 121023 | BAA10g12180 | A10 | 13642426 | G | A | upstream_gene_variant | MODIFIER | c.-287C>T| |
S263 |
| 121024 | BAA10g12180 | A10 | 13643119 | C | T | upstream_gene_variant | MODIFIER | c.-980G>A| |
S68 |
| 121025 | BAA10g12180 | A10 | 13646274 | G | A | upstream_gene_variant | MODIFIER | c.-4135C>T| |
S250 |