Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g18030 | A08 | 14538258 | C | T | upstream_gene_variant | MODIFIER | c.-4400C>T| |
S215 |
2 | BAA08g18030 | A08 | 14538330 | C | T | upstream_gene_variant | MODIFIER | c.-4328C>T| |
S167 |
3 | BAA08g18030 | A08 | 14539473 | G | A | upstream_gene_variant | MODIFIER | c.-3185G>A| |
S306 |
4 | BAA08g18030 | A08 | 14540232 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S302 |
5 | BAA08g18030 | A08 | 14541703 | C | T | upstream_gene_variant | MODIFIER | c.-955C>T| |
S271 |
6 | BAA08g18030 | A08 | 14541720 | G | A | upstream_gene_variant | MODIFIER | c.-938G>A| |
S67 |
7 | BAA08g18030 | A08 | 14542396 | C | T | upstream_gene_variant | MODIFIER | c.-262C>T| |
S178 |
8 | BAA08g18030 | A08 | 14542484 | C | T | upstream_gene_variant | MODIFIER | c.-174C>T| |
S19 |
9 | BAA08g18030 | A08 | 14543756 | G | A | missense_variant | MODERATE | c.581G>A|p.Ser194Asn |
S153 |
10 | BAA08g18030 | A08 | 14543770 | G | A | missense_variant | MODERATE | c.595G>A|p.Ala199Thr |
S65 |
11 | BAA08g18030 | A08 | 14545673 | G | A | stop_gained | HIGH | c.1250G>A|p.Trp417* |
S159 |
12 | BAA08g18030 | A08 | 14546472 | G | A | splice_region_variant&intron_variant | LOW | c.1666+7G>A| |
S262 |
13 | BAA08g18030 | A08 | 14546788 | C | T | missense_variant | MODERATE | c.1783C>T|p.Pro595Ser |
S247 |
14 | BAA08g18030 | A08 | 14546959 | C | T | missense_variant | MODERATE | c.1865C>T|p.Ser622Leu |
S51 |
15 | BAA08g18030 | A08 | 14546982 | C | T | missense_variant | MODERATE | c.1888C>T|p.Pro630Ser |
S303 |
16 | BAA08g18030 | A08 | 14547003 | C | T | missense_variant | MODERATE | c.1909C>T|p.Arg637Cys |
S275 |
17 | BAA08g18030 | A08 | 14547974 | G | A | downstream_gene_variant | MODIFIER | c.*948G>A| |
S193 |
18 | BAA08g18030 | A08 | 14548438 | G | A | downstream_gene_variant | MODIFIER | c.*1412G>A| |
S279 |