| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 138701 | BAA10g24160 | A10 | 20007819 | C | T | upstream_gene_variant | MODIFIER | c.-1070G>A| |
S162 |
| 138702 | BAA10g24170 | A10 | 20009311 | C | T | missense_variant | MODERATE | c.947C>T|p.Ser316Phe |
S11 |
| 138703 | BAA10g24160 | A10 | 20010238 | C | T | upstream_gene_variant | MODIFIER | c.-3489G>A| |
S67 |
| 138704 | BAA10g24160 | A10 | 20010590 | G | C | upstream_gene_variant | MODIFIER | c.-3841C>G| |
S299 |
| 138705 | BAA10g24160 | A10 | 20010614 | C | T | upstream_gene_variant | MODIFIER | c.-3865G>A| |
S218 |
| 138706 | BAA10g24180 | A10 | 20010970 | G | A | synonymous_variant | LOW | c.42G>A|p.Pro14Pro |
S293 |
| 138707 | BAA10g24180 | A10 | 20011247 | C | T | missense_variant | MODERATE | c.319C>T|p.His107Tyr |
S262 |
| 138708 | BAA10g24180 | A10 | 20011574 | G | A | missense_variant | MODERATE | c.646G>A|p.Asp216Asn |
S118 |
| 138709 | BAA10g24180 | A10 | 20011829 | G | A | missense_variant | MODERATE | c.901G>A|p.Asp301Asn |
S61 |
| 138710 | BAA10g24180 | A10 | 20012288 | C | T | synonymous_variant | LOW | c.1360C>T|p.Leu454Leu |
S124 |
| 138711 | BAA10g24180 | A10 | 20012411 | G | A | missense_variant | MODERATE | c.1483G>A|p.Glu495Lys |
S158 |
| 138712 | BAA10g24200 | A10 | 20013777 | G | A | upstream_gene_variant | MODIFIER | c.-3282G>A| |
S65 |
| 138713 | BAA10g24200 | A10 | 20013806 | G | A | upstream_gene_variant | MODIFIER | c.-3253G>A| |
S64 |
| 138714 | BAA10g24200 | A10 | 20014153 | G | A | upstream_gene_variant | MODIFIER | c.-2906G>A| |
S109 |
| 138715 | BAA10g24200 | A10 | 20014278 | C | T | upstream_gene_variant | MODIFIER | c.-2781C>T| |
S221 |
| 138716 | BAA10g24200 | A10 | 20014350 | G | A | upstream_gene_variant | MODIFIER | c.-2709G>A| |
S256 |
| 138717 | BAA10g24200 | A10 | 20014825 | C | T | upstream_gene_variant | MODIFIER | c.-2234C>T| |
S262 |
| 138718 | BAA10g24200 | A10 | 20015269 | G | A | upstream_gene_variant | MODIFIER | c.-1790G>A| |
S265 |
| 138719 | BAA10g24190 | A10 | 20015640 | G | A | synonymous_variant | LOW | c.648C>T|p.Arg216Arg |
S231 |
| 138720 | BAA10g24190 | A10 | 20015725 | G | A | missense_variant | MODERATE | c.563C>T|p.Ser188Phe |
S212 |
| 138721 | BAA10g24190 | A10 | 20015752 | G | A | missense_variant | MODERATE | c.536C>T|p.Ala179Val |
S231 |
| 138722 | BAA10g24200 | A10 | 20016531 | C | T | upstream_gene_variant | MODIFIER | c.-528C>T| |
S13 |
| 138723 | BAA10g24190 | A10 | 20019447 | G | A | upstream_gene_variant | MODIFIER | c.-2734C>T| |
S250 |
| 138724 | BAA10g24190 | A10 | 20020169 | G | A | upstream_gene_variant | MODIFIER | c.-3456C>T| |
S53 |
| 138725 | BAA10g24190 | A10 | 20020960 | G | A | upstream_gene_variant | MODIFIER | c.-4247C>T| |
S39 |