Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08030 | A10 | 5191132 | G | A | upstream_gene_variant | MODIFIER | c.-4556G>A| |
S217 S248 |
2 | BAA10g08030 | A10 | 5191320 | C | T | upstream_gene_variant | MODIFIER | c.-4368C>T| |
S177 |
3 | BAA10g08030 | A10 | 5191654 | C | T | upstream_gene_variant | MODIFIER | c.-4034C>T| |
S70 |
4 | BAA10g08030 | A10 | 5191754 | G | A | upstream_gene_variant | MODIFIER | c.-3934G>A| |
S115 |
5 | BAA10g08030 | A10 | 5191829 | C | T | upstream_gene_variant | MODIFIER | c.-3859C>T| |
S116 |
6 | BAA10g08030 | A10 | 5191903 | C | T | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S122 |
7 | BAA10g08030 | A10 | 5193032 | C | T | upstream_gene_variant | MODIFIER | c.-2656C>T| |
S1 S161 S228 S244 S290 S90 |
8 | BAA10g08030 | A10 | 5193782 | G | A | upstream_gene_variant | MODIFIER | c.-1906G>A| |
S283 |
9 | BAA10g08030 | A10 | 5193976 | G | A | upstream_gene_variant | MODIFIER | c.-1712G>A| |
S4 |
10 | BAA10g08030 | A10 | 5194971 | G | A | upstream_gene_variant | MODIFIER | c.-717G>A| |
S176 |
11 | BAA10g08030 | A10 | 5195043 | C | T | upstream_gene_variant | MODIFIER | c.-645C>T| |
S193 |
12 | BAA10g08030 | A10 | 5195181 | G | A | upstream_gene_variant | MODIFIER | c.-507G>A| |
S7 |
13 | BAA10g08030 | A10 | 5195535 | G | A | upstream_gene_variant | MODIFIER | c.-153G>A| |
S48 |
14 | BAA10g08030 | A10 | 5197355 | C | T | intron_variant | MODIFIER | c.1032+119C>T| |
S282 |
15 | BAA10g08030 | A10 | 5197999 | C | T | intron_variant | MODIFIER | c.1158+27C>T| |
S51 |
16 | BAA10g08030 | A10 | 5198144 | C | T | intron_variant | MODIFIER | c.1158+172C>T| |
S142 |
17 | BAA10g08030 | A10 | 5198148 | G | A | intron_variant | MODIFIER | c.1158+176G>A| |
S50 S51 |
18 | BAA10g08030 | A10 | 5198452 | G | A | intron_variant | MODIFIER | c.1158+480G>A| |
S212 |
19 | BAA10g08030 | A10 | 5198621 | G | A | intron_variant | MODIFIER | c.1159-642G>A| |
S234 |
20 | BAA10g08030 | A10 | 5199037 | G | A | intron_variant | MODIFIER | c.1159-226G>A| |
S69 |
21 | BAA10g08030 | A10 | 5199290 | G | A | missense_variant | MODERATE | c.1186G>A|p.Ala396Thr |
S245 |
22 | BAA10g08030 | A10 | 5199339 | C | A | missense_variant | MODERATE | c.1235C>A|p.Thr412Lys |
S185 |
23 | BAA10g08030 | A10 | 5199486 | G | A | synonymous_variant | LOW | c.1290G>A|p.Lys430Lys |
S192 |
24 | BAA10g08030 | A10 | 5199573 | G | A | stop_gained | HIGH | c.1377G>A|p.Trp459* |
S18 |
25 | BAA10g08030 | A10 | 5199657 | C | T | downstream_gene_variant | MODIFIER | c.*3C>T| |
S84 S93 |