| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 118101 | BAA10g10860 | A10 | 12604764 | G | A | intron_variant | MODIFIER | c.835-1120C>T| |
S59 |
| 118102 | BAA10g10860 | A10 | 12604830 | C | T | intron_variant | MODIFIER | c.835-1186G>A| |
S180 |
| 118103 | BAA10g10860 | A10 | 12604902 | G | A | intron_variant | MODIFIER | c.834+1149C>T| |
S207 |
| 118104 | BAA10g10860 | A10 | 12605245 | C | T | intron_variant | MODIFIER | c.834+806G>A| |
S275 |
| 118105 | BAA10g10860 | A10 | 12605247 | G | A | intron_variant | MODIFIER | c.834+804C>T| |
S292 |
| 118106 | BAA10g10860 | A10 | 12606287 | G | A | stop_gained | HIGH | c.598C>T|p.Gln200* |
S59 |
| 118107 | BAA10g10860 | A10 | 12607357 | G | A | intron_variant | MODIFIER | c.129-601C>T| |
S34 |
| 118108 | BAA10g10860 | A10 | 12607576 | G | A | intron_variant | MODIFIER | c.129-820C>T| |
S69 |
| 118109 | BAA10g10860 | A10 | 12608070 | C | T | intron_variant | MODIFIER | c.129-1314G>A| |
S123 |
| 118110 | BAA10g10860 | A10 | 12609969 | G | A | intron_variant | MODIFIER | c.128+2785C>T| |
S1 |
| 118111 | BAA10g10860 | A10 | 12610753 | G | A | intron_variant | MODIFIER | c.128+2001C>T| |
S228 |
| 118112 | BAA10g10860 | A10 | 12612224 | G | A | intron_variant | MODIFIER | c.128+530C>T| |
S241 |
| 118113 | BAA10g10860 | A10 | 12612760 | C | T | missense_variant | MODERATE | c.122G>A|p.Arg41Gln |
S10 |
| 118114 | BAA10g10860 | A10 | 12615683 | G | A | upstream_gene_variant | MODIFIER | c.-2802C>T| |
S259 S71 |
| 118115 | BAA10g10860 | A10 | 12616254 | C | T | upstream_gene_variant | MODIFIER | c.-3373G>A| |
S294 |
| 118116 | BAA10g10860 | A10 | 12616299 | G | A | upstream_gene_variant | MODIFIER | c.-3418C>T| |
S178 |
| 118117 | BAA10g10860 | A10 | 12616642 | C | T | upstream_gene_variant | MODIFIER | c.-3761G>A| |
S37 |
| 118118 | BAA10g10860 | A10 | 12617399 | G | A | upstream_gene_variant | MODIFIER | c.-4518C>T| |
S241 |
| 118119 | BAA10g10870 | A10 | 12618587 | G | A | synonymous_variant | LOW | c.393C>T|p.Asn131Asn |
S262 |
| 118120 | BAA10g10870 | A10 | 12618667 | G | A | missense_variant | MODERATE | c.313C>T|p.Pro105Ser |
S138 |
| 118121 | BAA10g10870 | A10 | 12620388 | C | T | upstream_gene_variant | MODIFIER | c.-1409G>A| |
S52 |
| 118122 | BAA10g10870 | A10 | 12621173 | C | T | upstream_gene_variant | MODIFIER | c.-2194G>A| |
S294 |
| 118123 | BAA10g10870 | A10 | 12622704 | G | A | upstream_gene_variant | MODIFIER | c.-3725C>T| |
S157 S163 S172 S217 |
| 118124 | BAA10g10870 | A10 | 12622726 | G | A | upstream_gene_variant | MODIFIER | c.-3747C>T| |
S67 |
| 118125 | BAA10g10870 | A10 | 12622876 | C | T | upstream_gene_variant | MODIFIER | c.-3897G>A| |
S144 |