Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05600 | A10 | 2875396 | G | A | upstream_gene_variant | MODIFIER | c.-4495G>A| |
S16 |
2 | BAA10g05600 | A10 | 2875580 | G | A | upstream_gene_variant | MODIFIER | c.-4311G>A| |
S15 S3 |
3 | BAA10g05600 | A10 | 2875655 | C | T | upstream_gene_variant | MODIFIER | c.-4236C>T| |
S131 |
4 | BAA10g05600 | A10 | 2875692 | G | A | upstream_gene_variant | MODIFIER | c.-4199G>A| |
S261 |
5 | BAA10g05600 | A10 | 2875812 | G | A | upstream_gene_variant | MODIFIER | c.-4079G>A| |
S174 S216 S241 S265 S27 S39 |
6 | BAA10g05600 | A10 | 2876075 | C | T | upstream_gene_variant | MODIFIER | c.-3816C>T| |
S287 |
7 | BAA10g05600 | A10 | 2877655 | C | T | upstream_gene_variant | MODIFIER | c.-2236C>T| |
S229 |
8 | BAA10g05600 | A10 | 2878345 | C | T | upstream_gene_variant | MODIFIER | c.-1546C>T| |
S204 |
9 | BAA10g05600 | A10 | 2879377 | C | T | upstream_gene_variant | MODIFIER | c.-514C>T| |
S225 |
10 | BAA10g05600 | A10 | 2879471 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S32 |
11 | BAA10g05600 | A10 | 2879647 | C | T | upstream_gene_variant | MODIFIER | c.-244C>T| |
S14 |
12 | BAA10g05600 | A10 | 2880129 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.185-1G>A| |
S133 |
13 | BAA10g05600 | A10 | 2880175 | G | A | stop_gained | HIGH | c.230G>A|p.Trp77* |
S55 |
14 | BAA10g05600 | A10 | 2880442 | C | T | missense_variant | MODERATE | c.497C>T|p.Ser166Phe |
S199 |
15 | BAA10g05600 | A10 | 2880447 | C | T | missense_variant | MODERATE | c.502C>T|p.Pro168Ser |
S28 |
16 | BAA10g05600 | A10 | 2880583 | G | A | missense_variant&splice_region_variant | MODERATE | c.544G>A|p.Ala182Thr |
S95 |