| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 95201 | BAA10g03980 | A10 | 1946079 | C | T | downstream_gene_variant | MODIFIER | c.*3898G>A| |
S256 |
| 95202 | BAA10g03980 | A10 | 1946108 | G | A | downstream_gene_variant | MODIFIER | c.*3869C>T| |
S276 |
| 95203 | BAA10g03970 | A10 | 1946539 | G | A | missense_variant | MODERATE | c.1430C>T|p.Ser477Phe |
S25 |
| 95204 | BAA10g03970 | A10 | 1946617 | C | T | missense_variant | MODERATE | c.1352G>A|p.Ser451Asn |
S60 |
| 95205 | BAA10g03980 | A10 | 1947058 | G | A | downstream_gene_variant | MODIFIER | c.*2919C>T| |
S33 |
| 95206 | BAA10g03980 | A10 | 1947188 | G | A | downstream_gene_variant | MODIFIER | c.*2789C>T| |
S251 |
| 95207 | BAA10g03970 | A10 | 1948034 | C | T | synonymous_variant | LOW | c.702G>A|p.Glu234Glu |
S305 |
| 95208 | BAA10g03970 | A10 | 1948530 | G | A | missense_variant | MODERATE | c.422C>T|p.Ala141Val |
S295 |
| 95209 | BAA10g03980 | A10 | 1949171 | C | T | downstream_gene_variant | MODIFIER | c.*806G>A| |
S142 |
| 95210 | BAA10g03980 | A10 | 1950533 | C | T | missense_variant | MODERATE | c.305G>A|p.Arg102Lys |
S271 S33 |
| 95211 | BAA10g03980 | A10 | 1950588 | C | T | missense_variant | MODERATE | c.250G>A|p.Glu84Lys |
S87 |
| 95212 | BAA10g03980 | A10 | 1950786 | C | T | missense_variant | MODERATE | c.52G>A|p.Asp18Asn |
S287 |
| 95213 | BAA10g03970 | A10 | 1950914 | C | T | upstream_gene_variant | MODIFIER | c.-1657G>A| |
S208 S93 |
| 95214 | BAA10g03970 | A10 | 1952759 | G | A | upstream_gene_variant | MODIFIER | c.-3502C>T| |
S55 |
| 95215 | BAA10g03970 | A10 | 1952879 | C | T | upstream_gene_variant | MODIFIER | c.-3622G>A| |
S67 |
| 95216 | BAA10g03970 | A10 | 1952957 | G | A | upstream_gene_variant | MODIFIER | c.-3700C>T| |
S112 |
| 95217 | BAA10g03970 | A10 | 1953020 | G | A | upstream_gene_variant | MODIFIER | c.-3763C>T| |
S162 |
| 95218 | BAA10g03970 | A10 | 1953073 | C | T | upstream_gene_variant | MODIFIER | c.-3816G>A| |
S10 |
| 95219 | BAA10g03970 | A10 | 1953239 | G | A | upstream_gene_variant | MODIFIER | c.-3982C>T| |
S71 |
| 95220 | BAA10g03970 | A10 | 1953656 | G | A | upstream_gene_variant | MODIFIER | c.-4399C>T| |
S217 S248 |
| 95221 | BAA10g03980 | A10 | 1955299 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S308 S79 |
| 95222 | BAA10g03990 | A10 | 1955931 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.332-1G>A| |
S13 |
| 95223 | BAA10g03990 | A10 | 1956873 | G | A | missense_variant | MODERATE | c.1273G>A|p.Gly425Ser |
S251 |
| 95224 | BAA10g03990 | A10 | 1957005 | G | A | missense_variant | MODERATE | c.1405G>A|p.Gly469Arg |
S219 S72 |
| 95225 | BAA10g03990 | A10 | 1957212 | G | A | missense_variant | MODERATE | c.1612G>A|p.Asp538Asn |
S60 |