| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 96001 | BAA10g04460 | A10 | 2246991 | G | A | upstream_gene_variant | MODIFIER | c.-596G>A| |
S242 |
| 96002 | BAA10g04460 | A10 | 2247261 | G | A | upstream_gene_variant | MODIFIER | c.-326G>A| |
S295 |
| 96003 | BAA10g04450 | A10 | 2247826 | C | T | downstream_gene_variant | MODIFIER | c.*4555C>T| |
S125 |
| 96004 | BAA10g04450 | A10 | 2248208 | G | A | downstream_gene_variant | MODIFIER | c.*4937G>A| |
S263 |
| 96005 | BAA10g04470 | A10 | 2249755 | A | T | downstream_gene_variant | MODIFIER | c.*3177T>A| |
S153 S213 |
| 96006 | BAA10g04470 | A10 | 2251943 | C | T | downstream_gene_variant | MODIFIER | c.*989G>A| |
S108 |
| 96007 | BAA10g04460 | A10 | 2252632 | G | A | downstream_gene_variant | MODIFIER | c.*207G>A| |
S120 |
| 96008 | BAA10g04470 | A10 | 2253198 | C | T | missense_variant | MODERATE | c.1153G>A|p.Glu385Lys |
S177 |
| 96009 | BAA10g04470 | A10 | 2253290 | C | T | missense_variant | MODERATE | c.1061G>A|p.Gly354Glu |
S225 S73 |
| 96010 | BAA10g04470 | A10 | 2253720 | G | A | synonymous_variant | LOW | c.631C>T|p.Leu211Leu |
S219 S72 |
| 96011 | BAA10g04470 | A10 | 2253995 | C | T | stop_gained | HIGH | c.356G>A|p.Trp119* |
S12 |
| 96012 | BAA10g04470 | A10 | 2254508 | C | T | upstream_gene_variant | MODIFIER | c.-158G>A| |
S143 |
| 96013 | BAA10g04470 | A10 | 2254534 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S149 |
| 96014 | BAA10g04470 | A10 | 2255984 | G | A | upstream_gene_variant | MODIFIER | c.-1634C>T| |
S95 |
| 96015 | BAA10g04480 | A10 | 2256515 | C | T | synonymous_variant | LOW | c.4971G>A|p.Lys1657Lys |
S271 |
| 96016 | BAA10g04470 | A10 | 2257205 | C | T | upstream_gene_variant | MODIFIER | c.-2855G>A| |
S37 |
| 96017 | BAA10g04480 | A10 | 2258281 | C | T | missense_variant | MODERATE | c.4303G>A|p.Val1435Ile |
S155 S211 |
| 96018 | BAA10g04470 | A10 | 2258544 | G | A | upstream_gene_variant | MODIFIER | c.-4194C>T| |
S25 |
| 96019 | BAA10g04480 | A10 | 2259220 | C | T | missense_variant | MODERATE | c.3794G>A|p.Ser1265Asn |
S108 |
| 96020 | BAA10g04480 | A10 | 2260797 | C | T | missense_variant | MODERATE | c.2875G>A|p.Glu959Lys |
S73 S91 |
| 96021 | BAA10g04480 | A10 | 2261944 | G | A | intron_variant | MODIFIER | c.2259+16C>T| |
S208 S219 |
| 96022 | BAA10g04480 | A10 | 2261974 | G | A | missense_variant | MODERATE | c.2245C>T|p.Arg749Cys |
S105 S106 |
| 96023 | BAA10g04480 | A10 | 2262160 | C | T | missense_variant | MODERATE | c.2143G>A|p.Val715Ile |
S23 |
| 96024 | BAA10g04480 | A10 | 2262917 | G | A | missense_variant | MODERATE | c.1748C>T|p.Thr583Ile |
S60 |
| 96025 | BAA10g04480 | A10 | 2262992 | G | A | missense_variant | MODERATE | c.1673C>T|p.Ala558Val |
S292 |