Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06960 | A10 | 3727071 | G | A | upstream_gene_variant | MODIFIER | c.-4413G>A| |
S279 |
2 | BAA10g06960 | A10 | 3727077 | G | A | upstream_gene_variant | MODIFIER | c.-4407G>A| |
S215 |
3 | BAA10g06960 | A10 | 3727202 | C | T | upstream_gene_variant | MODIFIER | c.-4282C>T| |
S143 |
4 | BAA10g06960 | A10 | 3727824 | G | A | upstream_gene_variant | MODIFIER | c.-3660G>A| |
S295 |
5 | BAA10g06960 | A10 | 3728003 | C | T | upstream_gene_variant | MODIFIER | c.-3481C>T| |
S143 |
6 | BAA10g06960 | A10 | 3728604 | G | A | upstream_gene_variant | MODIFIER | c.-2880G>A| |
S76 |
7 | BAA10g06960 | A10 | 3729022 | C | T | upstream_gene_variant | MODIFIER | c.-2462C>T| |
S56 |
8 | BAA10g06960 | A10 | 3733072 | G | A | intron_variant | MODIFIER | c.837+35G>A| |
S280 |
9 | BAA10g06960 | A10 | 3733134 | G | A | missense_variant | MODERATE | c.851G>A|p.Gly284Glu |
S85 |
10 | BAA10g06960 | A10 | 3733262 | G | A | missense_variant | MODERATE | c.979G>A|p.Glu327Lys |
S134 |
11 | BAA10g06960 | A10 | 3733702 | G | A | stop_gained | HIGH | c.1347G>A|p.Trp449* |
S7 |
12 | BAA10g06960 | A10 | 3734585 | C | T | downstream_gene_variant | MODIFIER | c.*856C>T| |
S44 |
13 | BAA10g06960 | A10 | 3737539 | G | A | downstream_gene_variant | MODIFIER | c.*3810G>A| |
S282 |
14 | BAA10g06960 | A10 | 3737618 | G | A | downstream_gene_variant | MODIFIER | c.*3889G>A| |
S263 |
15 | BAA10g06960 | A10 | 3737829 | C | T | downstream_gene_variant | MODIFIER | c.*4100C>T| |
S294 |
16 | BAA10g06960 | A10 | 3738010 | G | A | downstream_gene_variant | MODIFIER | c.*4281G>A| |
S1 S90 |
17 | BAA10g06960 | A10 | 3738192 | C | T | downstream_gene_variant | MODIFIER | c.*4463C>T| |
S308 |
18 | BAA10g06960 | A10 | 3738341 | C | T | downstream_gene_variant | MODIFIER | c.*4612C>T| |
S65 |
19 | BAA10g06960 | A10 | 3738681 | C | T | downstream_gene_variant | MODIFIER | c.*4952C>T| |
S42 |