| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 92401 | BAA10g02130 | A10 | 1002442 | C | T | upstream_gene_variant | MODIFIER | c.-843G>A| |
S182 |
| 92402 | BAA10g02130 | A10 | 1002993 | C | T | upstream_gene_variant | MODIFIER | c.-1394G>A| |
S44 |
| 92403 | BAA10g02130 | A10 | 1003415 | C | T | upstream_gene_variant | MODIFIER | c.-1816G>A| |
S287 |
| 92404 | BAA10g02130 | A10 | 1004032 | G | T | upstream_gene_variant | MODIFIER | c.-2433C>A| |
S76 |
| 92405 | BAA10g02130 | A10 | 1004076 | T | C | upstream_gene_variant | MODIFIER | c.-2477A>G| |
S250 |
| 92406 | BAA10g02140 | A10 | 1007346 | C | T | intron_variant | MODIFIER | c.513-154G>A| |
S235 |
| 92407 | BAA10g02140 | A10 | 1007568 | C | T | intron_variant | MODIFIER | c.513-376G>A| |
S170 |
| 92408 | BAA10g02140 | A10 | 1008064 | C | T | intron_variant | MODIFIER | c.513-872G>A| |
S61 |
| 92409 | BAA10g02140 | A10 | 1013135 | A | T | intron_variant | MODIFIER | c.512+2441T>A| |
S188 |
| 92410 | BAA10g02140 | A10 | 1013592 | T | A | intron_variant | MODIFIER | c.512+1984A>T| |
S169 |
| 92411 | BAA10g02140 | A10 | 1013722 | G | A | intron_variant | MODIFIER | c.512+1854C>T| |
S45 |
| 92412 | BAA10g02150 | A10 | 1015338 | A | T | upstream_gene_variant | MODIFIER | c.-4041A>T| |
S140 |
| 92413 | BAA10g02140 | A10 | 1015782 | C | T | synonymous_variant | LOW | c.306G>A|p.Gln102Gln |
S87 |
| 92414 | BAA10g02140 | A10 | 1016409 | G | A | upstream_gene_variant | MODIFIER | c.-322C>T| |
S289 |
| 92415 | BAA10g02140 | A10 | 1016820 | C | T | upstream_gene_variant | MODIFIER | c.-733G>A| |
S298 |
| 92416 | BAA10g02140 | A10 | 1018700 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S81 S85 |
| 92417 | BAA10g02140 | A10 | 1019201 | G | A | upstream_gene_variant | MODIFIER | c.-3114C>T| |
S265 |
| 92418 | BAA10g02140 | A10 | 1020004 | G | A | upstream_gene_variant | MODIFIER | c.-3917C>T| |
S205 |
| 92419 | BAA10g02150 | A10 | 1020427 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.415-1G>A| |
S13 |
| 92420 | BAA10g02140 | A10 | 1020616 | C | T | upstream_gene_variant | MODIFIER | c.-4529G>A| |
S8 |
| 92421 | BAA10g02140 | A10 | 1020856 | G | A | upstream_gene_variant | MODIFIER | c.-4769C>T| |
S290 |
| 92422 | BAA10g02150 | A10 | 1021171 | C | T | downstream_gene_variant | MODIFIER | c.*687C>T| |
S287 |
| 92423 | BAA10g02160 | A10 | 1026223 | C | T | missense_variant | MODERATE | c.11C>T|p.Ser4Phe |
S157 |
| 92424 | BAA10g02160 | A10 | 1026838 | C | T | missense_variant | MODERATE | c.626C>T|p.Pro209Leu |
S135 |
| 92425 | BAA10g02160 | A10 | 1026947 | C | T | synonymous_variant | LOW | c.735C>T|p.Leu245Leu |
S73 |