Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07170 | A10 | 3998586 | C | T | downstream_gene_variant | MODIFIER | c.*4663G>A| |
S56 |
2 | BAA10g07170 | A10 | 3998607 | C | T | downstream_gene_variant | MODIFIER | c.*4642G>A| |
S132 S137 S215 S89 |
3 | BAA10g07170 | A10 | 3998672 | C | T | downstream_gene_variant | MODIFIER | c.*4577G>A| |
S73 S91 |
4 | BAA10g07170 | A10 | 3999641 | C | T | downstream_gene_variant | MODIFIER | c.*3608G>A| |
S121 |
5 | BAA10g07170 | A10 | 3999767 | G | A | downstream_gene_variant | MODIFIER | c.*3482C>T| |
S128 |
6 | BAA10g07170 | A10 | 4000161 | G | A | downstream_gene_variant | MODIFIER | c.*3088C>T| |
S296 |
7 | BAA10g07170 | A10 | 4000878 | G | A | downstream_gene_variant | MODIFIER | c.*2371C>T| |
S128 |
8 | BAA10g07170 | A10 | 4002920 | C | T | downstream_gene_variant | MODIFIER | c.*329G>A| |
S144 |
9 | BAA10g07170 | A10 | 4003304 | G | A | missense_variant | MODERATE | c.1175C>T|p.Pro392Leu |
S308 |
10 | BAA10g07170 | A10 | 4003551 | C | T | missense_variant | MODERATE | c.928G>A|p.Glu310Lys |
S177 |
11 | BAA10g07170 | A10 | 4003639 | C | T | synonymous_variant | LOW | c.840G>A|p.Pro280Pro |
S282 |
12 | BAA10g07170 | A10 | 4004612 | C | T | synonymous_variant | LOW | c.159G>A|p.Gln53Gln |
S114 |
13 | BAA10g07170 | A10 | 4004710 | C | T | missense_variant | MODERATE | c.61G>A|p.Asp21Asn |
S202 |
14 | BAA10g07170 | A10 | 4004827 | G | A | upstream_gene_variant | MODIFIER | c.-57C>T| |
S174 S216 S241 S265 S27 S39 |
15 | BAA10g07170 | A10 | 4005883 | G | A | upstream_gene_variant | MODIFIER | c.-1113C>T| |
S20 |
16 | BAA10g07170 | A10 | 4006648 | C | T | upstream_gene_variant | MODIFIER | c.-1878G>A| |
S297 |
17 | BAA10g07170 | A10 | 4007057 | C | T | upstream_gene_variant | MODIFIER | c.-2287G>A| |
S23 |
18 | BAA10g07170 | A10 | 4008241 | C | T | upstream_gene_variant | MODIFIER | c.-3471G>A| |
S263 |
19 | BAA10g07170 | A10 | 4008917 | C | T | upstream_gene_variant | MODIFIER | c.-4147G>A| |
S25 |
20 | BAA10g07170 | A10 | 4008962 | C | T | upstream_gene_variant | MODIFIER | c.-4192G>A| |
S185 |