| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 112101 | BAA10g08430 | A10 | 10236018 | C | T | splice_region_variant&intron_variant | LOW | c.1028+7C>T| |
S122 |
| 112102 | BAA10g08440 | A10 | 10236634 | G | A | downstream_gene_variant | MODIFIER | c.*3279C>T| |
S43 |
| 112103 | BAA10g08430 | A10 | 10237085 | C | T | stop_gained | HIGH | c.1045C>T|p.Arg349* |
S167 |
| 112104 | BAA10g08430 | A10 | 10237331 | G | A | missense_variant | MODERATE | c.1199G>A|p.Gly400Glu |
S88 |
| 112105 | BAA10g08430 | A10 | 10237494 | G | A | synonymous_variant | LOW | c.1362G>A|p.Gly454Gly |
S15 S3 |
| 112106 | BAA10g08430 | A10 | 10237538 | C | T | missense_variant | MODERATE | c.1406C>T|p.Thr469Ile |
S189 |
| 112107 | BAA10g08430 | A10 | 10238403 | G | A | missense_variant | MODERATE | c.2023G>A|p.Glu675Lys |
S25 |
| 112108 | BAA10g08440 | A10 | 10239996 | G | A | synonymous_variant | LOW | c.169C>T|p.Leu57Leu |
S76 |
| 112109 | BAA10g08440 | A10 | 10240145 | G | A | missense_variant | MODERATE | c.20C>T|p.Ser7Phe |
S156 |
| 112110 | BAA10g08440 | A10 | 10240812 | G | A | upstream_gene_variant | MODIFIER | c.-648C>T| |
S88 |
| 112111 | BAA10g08440 | A10 | 10241006 | G | A | upstream_gene_variant | MODIFIER | c.-842C>T| |
S139 |
| 112112 | BAA10g08440 | A10 | 10241236 | G | A | upstream_gene_variant | MODIFIER | c.-1072C>T| |
S64 |
| 112113 | BAA10g08440 | A10 | 10241268 | G | A | upstream_gene_variant | MODIFIER | c.-1104C>T| |
S202 |
| 112114 | BAA10g08440 | A10 | 10242453 | G | A | upstream_gene_variant | MODIFIER | c.-2289C>T| |
S250 |
| 112115 | BAA10g08450 | A10 | 10242625 | G | A | missense_variant | MODERATE | c.1700C>T|p.Ala567Val |
S279 |
| 112116 | BAA10g08450 | A10 | 10243077 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1249-1G>A| |
S83 S88 |
| 112117 | BAA10g08450 | A10 | 10243900 | G | A | synonymous_variant | LOW | c.852C>T|p.Ile284Ile |
S18 |
| 112118 | BAA10g08450 | A10 | 10244195 | G | A | missense_variant | MODERATE | c.557C>T|p.Ser186Phe |
S79 S84 |
| 112119 | BAA10g08450 | A10 | 10244636 | C | T | synonymous_variant | LOW | c.192G>A|p.Ala64Ala |
S42 |
| 112120 | BAA10g08450 | A10 | 10247325 | G | A | upstream_gene_variant | MODIFIER | c.-2311C>T| |
S55 |
| 112121 | BAA10g08450 | A10 | 10247749 | G | A | upstream_gene_variant | MODIFIER | c.-2735C>T| |
S4 |
| 112122 | BAA10g08450 | A10 | 10247883 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S44 |
| 112123 | BAA10g08460 | A10 | 10250196 | G | A | stop_gained | HIGH | c.362G>A|p.Trp121* |
S306 |
| 112124 | BAA10g08470 | A10 | 10251221 | C | T | upstream_gene_variant | MODIFIER | c.-614C>T| |
S203 |
| 112125 | BAA10g08470 | A10 | 10252837 | G | A | synonymous_variant | LOW | c.666G>A|p.Ala222Ala |
S62 |