Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07080 | A10 | 3917210 | G | A | upstream_gene_variant | MODIFIER | c.-4607G>A| |
S23 |
2 | BAA10g07080 | A10 | 3917244 | G | A | upstream_gene_variant | MODIFIER | c.-4573G>A| |
S103 |
3 | BAA10g07080 | A10 | 3917457 | G | A | upstream_gene_variant | MODIFIER | c.-4360G>A| |
S306 S308 |
4 | BAA10g07080 | A10 | 3917762 | C | T | upstream_gene_variant | MODIFIER | c.-4055C>T| |
S183 |
5 | BAA10g07080 | A10 | 3917855 | G | A | upstream_gene_variant | MODIFIER | c.-3962G>A| |
S217 S248 |
6 | BAA10g07080 | A10 | 3920923 | C | T | upstream_gene_variant | MODIFIER | c.-894C>T| |
S270 |
7 | BAA10g07080 | A10 | 3921944 | G | A | missense_variant | MODERATE | c.128G>A|p.Gly43Glu |
S292 |
8 | BAA10g07080 | A10 | 3921967 | C | T | missense_variant | MODERATE | c.151C>T|p.Pro51Ser |
S12 |
9 | BAA10g07080 | A10 | 3923619 | G | A | synonymous_variant | LOW | c.1731G>A|p.Leu577Leu |
S12 |
10 | BAA10g07080 | A10 | 3923650 | G | A | missense_variant | MODERATE | c.1762G>A|p.Asp588Asn |
S221 |
11 | BAA10g07080 | A10 | 3924167 | G | A | splice_region_variant&stop_retained_variant | LOW | c.2279G>A|p.Ter760Ter |
S161 |
12 | BAA10g07080 | A10 | 3924798 | C | T | downstream_gene_variant | MODIFIER | c.*630C>T| |
S42 |
13 | BAA10g07080 | A10 | 3924943 | C | T | downstream_gene_variant | MODIFIER | c.*775C>T| |
S176 |
14 | BAA10g07080 | A10 | 3925867 | C | T | downstream_gene_variant | MODIFIER | c.*1699C>T| |
S84 S93 |
15 | BAA10g07080 | A10 | 3926063 | G | A | downstream_gene_variant | MODIFIER | c.*1895G>A| |
S302 |
16 | BAA10g07080 | A10 | 3926365 | G | A | downstream_gene_variant | MODIFIER | c.*2197G>A| |
S18 |
17 | BAA10g07080 | A10 | 3927298 | G | A | downstream_gene_variant | MODIFIER | c.*3130G>A| |
S298 |
18 | BAA10g07080 | A10 | 3928119 | G | A | downstream_gene_variant | MODIFIER | c.*3951G>A| |
S178 |