Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14630 | A09 | 8329635 | C | T | upstream_gene_variant | MODIFIER | c.-4237C>T| |
S270 |
2 | BAA09g14630 | A09 | 8330134 | G | A | upstream_gene_variant | MODIFIER | c.-3738G>A| |
S202 |
3 | BAA09g14630 | A09 | 8330481 | C | T | upstream_gene_variant | MODIFIER | c.-3391C>T| |
S133 |
4 | BAA09g14630 | A09 | 8331179 | C | T | upstream_gene_variant | MODIFIER | c.-2693C>T| |
S135 |
5 | BAA09g14630 | A09 | 8332558 | G | A | upstream_gene_variant | MODIFIER | c.-1314G>A| |
S244 |
6 | BAA09g14630 | A09 | 8332612 | G | A | upstream_gene_variant | MODIFIER | c.-1260G>A| |
S233 |
7 | BAA09g14630 | A09 | 8333429 | G | A | upstream_gene_variant | MODIFIER | c.-443G>A| |
S182 |
8 | BAA09g14630 | A09 | 8334005 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.70-1G>A| |
S166 |
9 | BAA09g14630 | A09 | 8334503 | G | A | missense_variant | MODERATE | c.493G>A|p.Asp165Asn |
S146 |
10 | BAA09g14630 | A09 | 8334664 | C | T | synonymous_variant | LOW | c.558C>T|p.Ser186Ser |
S231 |
11 | BAA09g14630 | A09 | 8334979 | G | A | stop_gained | HIGH | c.873G>A|p.Trp291* |
S200 |
12 | BAA09g14630 | A09 | 8335855 | C | T | downstream_gene_variant | MODIFIER | c.*753C>T| |
S105 S80 |
13 | BAA09g14630 | A09 | 8336387 | G | A | downstream_gene_variant | MODIFIER | c.*1285G>A| |
S1 S90 |
14 | BAA09g14630 | A09 | 8337164 | C | T | downstream_gene_variant | MODIFIER | c.*2062C>T| |
S149 |
15 | BAA09g14630 | A09 | 8337662 | G | A | downstream_gene_variant | MODIFIER | c.*2560G>A| |
S87 |
16 | BAA09g14630 | A09 | 8338009 | C | T | downstream_gene_variant | MODIFIER | c.*2907C>T| |
S287 |
17 | BAA09g14630 | A09 | 8339147 | G | A | downstream_gene_variant | MODIFIER | c.*4045G>A| |
S166 |
18 | BAA09g14630 | A09 | 8339873 | C | T | downstream_gene_variant | MODIFIER | c.*4771C>T| |
S111 |