Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22190 | A08 | 16745249 | G | A | upstream_gene_variant | MODIFIER | c.-4289G>A| |
S76 |
2 | BAA08g22190 | A08 | 16746340 | C | T | upstream_gene_variant | MODIFIER | c.-3198C>T| |
S6 |
3 | BAA08g22190 | A08 | 16747597 | G | A | upstream_gene_variant | MODIFIER | c.-1941G>A| |
S245 |
4 | BAA08g22190 | A08 | 16747610 | C | T | upstream_gene_variant | MODIFIER | c.-1928C>T| |
S251 |
5 | BAA08g22190 | A08 | 16748486 | G | A | upstream_gene_variant | MODIFIER | c.-1052G>A| |
S287 |
6 | BAA08g22190 | A08 | 16748689 | C | T | upstream_gene_variant | MODIFIER | c.-849C>T| |
S237 |
7 | BAA08g22190 | A08 | 16749295 | C | T | upstream_gene_variant | MODIFIER | c.-243C>T| |
S223 |
8 | BAA08g22190 | A08 | 16749846 | C | T | missense_variant | MODERATE | c.145C>T|p.Pro49Ser |
S81 S85 |
9 | BAA08g22190 | A08 | 16750043 | G | A | intron_variant | MODIFIER | c.178-39G>A| |
S40 S49 |
10 | BAA08g22190 | A08 | 16750287 | G | A | intron_variant | MODIFIER | c.293+90G>A| |
S266 |
11 | BAA08g22190 | A08 | 16751602 | G | A | intron_variant | MODIFIER | c.786+161G>A| |
S162 |
12 | BAA08g22190 | A08 | 16752532 | C | T | intron_variant | MODIFIER | c.1040+19C>T| |
S233 |
13 | BAA08g22190 | A08 | 16752709 | C | T | synonymous_variant | LOW | c.1122C>T|p.Thr374Thr |
S274 |
14 | BAA08g22190 | A08 | 16754731 | G | A | intron_variant | MODIFIER | c.1560-243G>A| |
S229 |
15 | BAA08g22190 | A08 | 16756491 | G | A | missense_variant | MODERATE | c.1874G>A|p.Gly625Glu |
S195 |
16 | BAA08g22190 | A08 | 16756746 | G | A | missense_variant | MODERATE | c.1987G>A|p.Ala663Thr |
S91 |
17 | BAA08g22190 | A08 | 16757944 | C | T | intron_variant | MODIFIER | c.2508-28C>T| |
S167 |
18 | BAA08g22190 | A08 | 16758039 | G | A | missense_variant | MODERATE | c.2575G>A|p.Gly859Ser |
S20 |
19 | BAA08g22190 | A08 | 16758712 | C | T | intron_variant | MODIFIER | c.2599-466C>T| |
S277 |
20 | BAA08g22190 | A08 | 16759533 | C | T | synonymous_variant | LOW | c.2875C>T|p.Leu959Leu |
S215 |
21 | BAA08g22190 | A08 | 16760678 | C | T | downstream_gene_variant | MODIFIER | c.*462C>T| |
S118 |
22 | BAA08g22190 | A08 | 16761010 | C | T | downstream_gene_variant | MODIFIER | c.*794C>T| |
S293 |