Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g33860 | A06 | 22831757 | G | A | upstream_gene_variant | MODIFIER | c.-4367G>A| |
S73 |
2 | BAA06g33860 | A06 | 22832186 | C | T | upstream_gene_variant | MODIFIER | c.-3938C>T| |
S116 |
3 | BAA06g33860 | A06 | 22832357 | G | A | upstream_gene_variant | MODIFIER | c.-3767G>A| |
S161 S244 S289 S290 |
4 | BAA06g33860 | A06 | 22832712 | G | A | upstream_gene_variant | MODIFIER | c.-3412G>A| |
S250 |
5 | BAA06g33860 | A06 | 22832816 | C | T | upstream_gene_variant | MODIFIER | c.-3308C>T| |
S223 |
6 | BAA06g33860 | A06 | 22833890 | G | A | upstream_gene_variant | MODIFIER | c.-2234G>A| |
S169 |
7 | BAA06g33860 | A06 | 22834623 | C | T | upstream_gene_variant | MODIFIER | c.-1501C>T| |
S10 |
8 | BAA06g33860 | A06 | 22834635 | C | T | upstream_gene_variant | MODIFIER | c.-1489C>T| |
S247 |
9 | BAA06g33860 | A06 | 22834792 | G | A | upstream_gene_variant | MODIFIER | c.-1332G>A| |
S60 |
10 | BAA06g33860 | A06 | 22834891 | G | A | upstream_gene_variant | MODIFIER | c.-1233G>A| |
S208 S219 |
11 | BAA06g33860 | A06 | 22835629 | G | A | upstream_gene_variant | MODIFIER | c.-495G>A| |
S297 |
12 | BAA06g33860 | A06 | 22836399 | G | A | synonymous_variant | LOW | c.210G>A|p.Thr70Thr |
S117 |
13 | BAA06g33860 | A06 | 22836609 | C | T | missense_variant | MODERATE | c.305C>T|p.Ala102Val |
S82 S92 |
14 | BAA06g33860 | A06 | 22836756 | C | T | missense_variant | MODERATE | c.452C>T|p.Ser151Phe |
S108 |
15 | BAA06g33860 | A06 | 22837110 | C | T | synonymous_variant | LOW | c.666C>T|p.Thr222Thr |
S239 |
16 | BAA06g33860 | A06 | 22837129 | G | A | missense_variant | MODERATE | c.685G>A|p.Asp229Asn |
S194 |
17 | BAA06g33860 | A06 | 22837202 | G | A | missense_variant | MODERATE | c.758G>A|p.Gly253Glu |
S133 |
18 | BAA06g33860 | A06 | 22837839 | G | A | splice_region_variant&synonymous_variant | LOW | c.1290G>A|p.Val430Val |
S63 |
19 | BAA06g33860 | A06 | 22837939 | C | T | missense_variant | MODERATE | c.1390C>T|p.Pro464Ser |
S96 |
20 | BAA06g33860 | A06 | 22838378 | C | T | missense_variant | MODERATE | c.1604C>T|p.Ser535Phe |
S74 |
21 | BAA06g33860 | A06 | 22838920 | G | A | missense_variant | MODERATE | c.1808G>A|p.Gly603Glu |
S117 |
22 | BAA06g33860 | A06 | 22840491 | C | T | missense_variant | MODERATE | c.3038C>T|p.Pro1013Leu |
S120 |
23 | BAA06g33860 | A06 | 22842683 | C | T | downstream_gene_variant | MODIFIER | c.*2086C>T| |
S117 |
24 | BAA06g33860 | A06 | 22843255 | C | T | downstream_gene_variant | MODIFIER | c.*2658C>T| |
S252 |
25 | BAA06g33860 | A06 | 22844488 | C | T | downstream_gene_variant | MODIFIER | c.*3891C>T| |
S130 |