| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 131951 | BAA10g19040 | A10 | 17614013 | G | A | upstream_gene_variant | MODIFIER | c.-2859C>T| |
S278 |
| 131952 | BAA10g19040 | A10 | 17614169 | C | T | upstream_gene_variant | MODIFIER | c.-3015G>A| |
S2 S213 S3 S4 S6 |
| 131953 | BAA10g19040 | A10 | 17614443 | G | A | upstream_gene_variant | MODIFIER | c.-3289C>T| |
S208 S219 |
| 131954 | BAA10g19040 | A10 | 17614470 | G | A | upstream_gene_variant | MODIFIER | c.-3316C>T| |
S158 |
| 131955 | BAA10g19040 | A10 | 17614659 | G | A | upstream_gene_variant | MODIFIER | c.-3505C>T| |
S293 |
| 131956 | BAA10g19040 | A10 | 17614667 | G | A | upstream_gene_variant | MODIFIER | c.-3513C>T| |
S79 S84 |
| 131957 | BAA10g19040 | A10 | 17614881 | G | A | upstream_gene_variant | MODIFIER | c.-3727C>T| |
S88 |
| 131958 | BAA10g19040 | A10 | 17615357 | C | T | upstream_gene_variant | MODIFIER | c.-4203G>A| |
S191 |
| 131959 | BAA10g19040 | A10 | 17615427 | G | A | upstream_gene_variant | MODIFIER | c.-4273C>T| |
S105 S106 |
| 131960 | BAA10g19050 | A10 | 17615940 | G | A | missense_variant | MODERATE | c.185G>A|p.Gly62Glu |
S262 |
| 131961 | BAA10g19050 | A10 | 17616480 | C | T | intron_variant | MODIFIER | c.516+95C>T| |
S174 S216 S265 |
| 131962 | BAA10g19050 | A10 | 17616590 | G | A | missense_variant | MODERATE | c.520G>A|p.Asp174Asn |
S264 |
| 131963 | BAA10g19050 | A10 | 17616597 | G | A | missense_variant | MODERATE | c.527G>A|p.Arg176Lys |
S250 |
| 131964 | BAA10g19050 | A10 | 17616683 | G | A | missense_variant | MODERATE | c.613G>A|p.Glu205Lys |
S4 |
| 131965 | BAA10g19050 | A10 | 17617333 | C | T | missense_variant | MODERATE | c.827C>T|p.Ser276Phe |
S269 |
| 131966 | BAA10g19050 | A10 | 17617646 | G | A | missense_variant | MODERATE | c.1036G>A|p.Val346Ile |
S155 |
| 131967 | BAA10g19050 | A10 | 17618403 | C | T | splice_region_variant&intron_variant | LOW | c.1605-8C>T| |
S190 |
| 131968 | BAA10g19060 | A10 | 17618659 | G | A | upstream_gene_variant | MODIFIER | c.-3521G>A| |
S192 |
| 131969 | BAA10g19050 | A10 | 17618787 | G | A | missense_variant | MODERATE | c.1720G>A|p.Asp574Asn |
S181 |
| 131970 | BAA10g19050 | A10 | 17619261 | C | T | missense_variant | MODERATE | c.1936C>T|p.Pro646Ser |
S46 |
| 131971 | BAA10g19050 | A10 | 17619735 | C | T | synonymous_variant | LOW | c.2410C>T|p.Leu804Leu |
S135 |
| 131972 | BAA10g19050 | A10 | 17619777 | C | T | missense_variant | MODERATE | c.2452C>T|p.Pro818Ser |
S260 |
| 131973 | BAA10g19060 | A10 | 17620091 | G | A | upstream_gene_variant | MODIFIER | c.-2089G>A| |
S180 |
| 131974 | BAA10g19060 | A10 | 17621660 | C | T | upstream_gene_variant | MODIFIER | c.-520C>T| |
S46 |
| 131975 | BAA10g19060 | A10 | 17621854 | C | T | upstream_gene_variant | MODIFIER | c.-326C>T| |
S5 |