| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 143351 | BAA10g28130 | A10 | 21674322 | C | T | intron_variant | MODIFIER | c.414+16C>T| |
S247 |
| 143352 | BAA10g28130 | A10 | 21674391 | G | A | missense_variant | MODERATE | c.422G>A|p.Gly141Glu |
S202 |
| 143353 | BAA10g28140 | A10 | 21675531 | C | T | upstream_gene_variant | MODIFIER | c.-3950C>T| |
S44 |
| 143354 | BAA10g28140 | A10 | 21678902 | G | A | upstream_gene_variant | MODIFIER | c.-579G>A| |
S160 |
| 143355 | BAA10g28150 | A10 | 21679933 | G | A | upstream_gene_variant | MODIFIER | c.-1503G>A| |
S139 |
| 143356 | BAA10g28150 | A10 | 21684832 | C | T | missense_variant | MODERATE | c.701C>T|p.Thr234Ile |
S187 |
| 143357 | BAA10g28150 | A10 | 21685377 | G | A | missense_variant | MODERATE | c.955G>A|p.Gly319Ser |
S280 |
| 143358 | BAA10g28150 | A10 | 21685495 | C | T | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S294 |
| 143359 | BAA10g28150 | A10 | 21685581 | C | T | missense_variant | MODERATE | c.1159C>T|p.Leu387Phe |
S161 |
| 143360 | BAA10g28160 | A10 | 21686115 | G | A | upstream_gene_variant | MODIFIER | c.-954G>A| |
S240 |
| 143361 | BAA10g28160 | A10 | 21686894 | G | A | upstream_gene_variant | MODIFIER | c.-175G>A| |
S16 |
| 143362 | BAA10g28160 | A10 | 21686935 | G | A | upstream_gene_variant | MODIFIER | c.-134G>A| |
S35 |
| 143363 | BAA10g28160 | A10 | 21687058 | G | A | upstream_gene_variant | MODIFIER | c.-11G>A| |
S32 |
| 143364 | BAA10g28160 | A10 | 21687681 | C | T | missense_variant | MODERATE | c.532C>T|p.Leu178Phe |
S295 |
| 143365 | BAA10g28160 | A10 | 21688710 | G | A | missense_variant | MODERATE | c.995G>A|p.Arg332Gln |
S165 S211 S227 |
| 143366 | BAA10g28160 | A10 | 21689088 | G | A | stop_gained | HIGH | c.1290G>A|p.Trp430* |
S286 |
| 143367 | BAA10g28170 | A10 | 21689997 | C | T | upstream_gene_variant | MODIFIER | c.-615C>T| |
S225 |
| 143368 | BAA10g28170 | A10 | 21690997 | G | A | missense_variant | MODERATE | c.299G>A|p.Ser100Asn |
S262 |
| 143369 | BAA10g28170 | A10 | 21692433 | G | A | missense_variant | MODERATE | c.1223G>A|p.Gly408Glu |
S74 |
| 143370 | BAA10g28190 | A10 | 21692601 | C | T | upstream_gene_variant | MODIFIER | c.-2483C>T| |
S168 |
| 143371 | BAA10g28190 | A10 | 21693510 | G | A | upstream_gene_variant | MODIFIER | c.-1574G>A| |
S190 |
| 143372 | BAA10g28180 | A10 | 21693697 | G | A | missense_variant | MODERATE | c.593C>T|p.Ser198Leu |
S219 S72 |
| 143373 | BAA10g28190 | A10 | 21693743 | G | A | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S158 |
| 143374 | BAA10g28190 | A10 | 21693874 | C | T | upstream_gene_variant | MODIFIER | c.-1210C>T| |
S33 |
| 143375 | BAA10g28180 | A10 | 21694153 | C | T | missense_variant | MODERATE | c.370G>A|p.Val124Ile |
S195 |