| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 95051 | BAA10g03870 | A10 | 1887823 | C | T | missense_variant | MODERATE | c.484C>T|p.Pro162Ser |
S199 |
| 95052 | BAA10g03870 | A10 | 1888557 | A | T | downstream_gene_variant | MODIFIER | c.*204A>T| |
S128 |
| 95053 | BAA10g03880 | A10 | 1891140 | G | A | synonymous_variant | LOW | c.1408C>T|p.Leu470Leu |
S240 |
| 95054 | BAA10g03880 | A10 | 1891492 | G | A | missense_variant | MODERATE | c.1249C>T|p.Arg417Cys |
S167 |
| 95055 | BAA10g03880 | A10 | 1892341 | G | A | synonymous_variant | LOW | c.561C>T|p.Arg187Arg |
S15 |
| 95056 | BAA10g03880 | A10 | 1892533 | C | T | synonymous_variant | LOW | c.369G>A|p.Leu123Leu |
S287 |
| 95057 | BAA10g03880 | A10 | 1892736 | C | T | missense_variant | MODERATE | c.166G>A|p.Asp56Asn |
S205 |
| 95058 | BAA10g03880 | A10 | 1892758 | C | T | synonymous_variant | LOW | c.144G>A|p.Glu48Glu |
S135 |
| 95059 | BAA10g03880 | A10 | 1893506 | C | T | upstream_gene_variant | MODIFIER | c.-383G>A| |
S185 |
| 95060 | BAA10g03880 | A10 | 1893594 | C | T | upstream_gene_variant | MODIFIER | c.-471G>A| |
S176 |
| 95061 | BAA10g03880 | A10 | 1895112 | C | T | upstream_gene_variant | MODIFIER | c.-1989G>A| |
S244 |
| 95062 | BAA10g03880 | A10 | 1896648 | G | A | upstream_gene_variant | MODIFIER | c.-3525C>T| |
S226 |
| 95063 | BAA10g03890 | A10 | 1899141 | C | T | downstream_gene_variant | MODIFIER | c.*3817G>A| |
S25 |
| 95064 | BAA10g03890 | A10 | 1899464 | G | A | downstream_gene_variant | MODIFIER | c.*3494C>T| |
S257 |
| 95065 | BAA10g03890 | A10 | 1899485 | C | T | downstream_gene_variant | MODIFIER | c.*3473G>A| |
S177 |
| 95066 | BAA10g03890 | A10 | 1900720 | C | T | downstream_gene_variant | MODIFIER | c.*2238G>A| |
S42 |
| 95067 | BAA10g03890 | A10 | 1900972 | G | A | downstream_gene_variant | MODIFIER | c.*1986C>T| |
S278 |
| 95068 | BAA10g03890 | A10 | 1901171 | G | A | downstream_gene_variant | MODIFIER | c.*1787C>T| |
S242 |
| 95069 | BAA10g03890 | A10 | 1901663 | G | A | downstream_gene_variant | MODIFIER | c.*1295C>T| |
S13 |
| 95070 | BAA10g03890 | A10 | 1901832 | C | T | downstream_gene_variant | MODIFIER | c.*1126G>A| |
S143 |
| 95071 | BAA10g03890 | A10 | 1902257 | G | A | downstream_gene_variant | MODIFIER | c.*701C>T| |
S120 |
| 95072 | BAA10g03890 | A10 | 1902456 | G | A | downstream_gene_variant | MODIFIER | c.*502C>T| |
S16 |
| 95073 | BAA10g03890 | A10 | 1903130 | C | T | intron_variant | MODIFIER | c.70-35G>A| |
S104 S52 |
| 95074 | BAA10g03890 | A10 | 1904147 | G | A | intron_variant | MODIFIER | c.69+44C>T| |
S156 |
| 95075 | BAA10g03890 | A10 | 1904724 | C | T | upstream_gene_variant | MODIFIER | c.-465G>A| |
S247 |