| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 91501 | BAA10g01430 | A10 | 723601 | G | A | upstream_gene_variant | MODIFIER | c.-67C>T| |
S15 |
| 91502 | BAA10g01430 | A10 | 724097 | C | T | upstream_gene_variant | MODIFIER | c.-563G>A| |
S135 |
| 91503 | BAA10g01430 | A10 | 724731 | G | A | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S40 S49 |
| 91504 | BAA10g01430 | A10 | 726983 | G | A | upstream_gene_variant | MODIFIER | c.-3449C>T| |
S240 |
| 91505 | BAA10g01430 | A10 | 728188 | G | A | upstream_gene_variant | MODIFIER | c.-4654C>T| |
S151 S263 |
| 91506 | BAA10g01430 | A10 | 728521 | G | A | upstream_gene_variant | MODIFIER | c.-4987C>T| |
S60 |
| 91507 | BAA10g01440 | A10 | 730025 | C | T | upstream_gene_variant | MODIFIER | c.-114C>T| |
S144 |
| 91508 | BAA10g01440 | A10 | 730406 | G | A | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S274 |
| 91509 | BAA10g01440 | A10 | 730440 | G | A | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S217 S248 |
| 91510 | BAA10g01450 | A10 | 731164 | C | T | upstream_gene_variant | MODIFIER | c.-2835C>T| |
S75 S81 |
| 91511 | BAA10g01440 | A10 | 731319 | C | T | missense_variant | MODERATE | c.455C>T|p.Thr152Ile |
S175 |
| 91512 | BAA10g01440 | A10 | 731387 | G | A | missense_variant | MODERATE | c.523G>A|p.Glu175Lys |
S303 |
| 91513 | BAA10g01440 | A10 | 732260 | C | T | missense_variant | MODERATE | c.1106C>T|p.Pro369Leu |
S60 |
| 91514 | BAA10g01440 | A10 | 732555 | G | A | synonymous_variant | LOW | c.1401G>A|p.Arg467Arg |
S228 |
| 91515 | BAA10g01440 | A10 | 732568 | G | A | missense_variant | MODERATE | c.1414G>A|p.Ala472Thr |
S151 S263 |
| 91516 | BAA10g01440 | A10 | 732586 | G | A | missense_variant | MODERATE | c.1432G>A|p.Gly478Arg |
S76 |
| 91517 | BAA10g01440 | A10 | 733372 | C | T | missense_variant | MODERATE | c.2218C>T|p.Pro740Ser |
S294 |
| 91518 | BAA10g01450 | A10 | 733553 | G | A | upstream_gene_variant | MODIFIER | c.-446G>A| |
S250 |
| 91519 | BAA10g01450 | A10 | 733710 | G | A | upstream_gene_variant | MODIFIER | c.-289G>A| |
S296 |
| 91520 | BAA10g01470 | A10 | 734275 | C | T | upstream_gene_variant | MODIFIER | c.-3928C>T| |
S146 |
| 91521 | BAA10g01450 | A10 | 734403 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.142-1G>A| |
S164 |
| 91522 | BAA10g01450 | A10 | 734596 | G | A | missense_variant | MODERATE | c.224G>A|p.Gly75Asp |
S18 |
| 91523 | BAA10g01470 | A10 | 734856 | C | T | upstream_gene_variant | MODIFIER | c.-3347C>T| |
S294 |
| 91524 | BAA10g01460 | A10 | 737033 | C | T | upstream_gene_variant | MODIFIER | c.-1365G>A| |
S246 |
| 91525 | BAA10g01460 | A10 | 737978 | G | A | upstream_gene_variant | MODIFIER | c.-2310C>T| |
S133 |