Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g08960 | A08 | 8181412 | C | T | upstream_gene_variant | MODIFIER | c.-3352C>T| |
S140 |
2 | BAA08g08960 | A08 | 8182065 | G | A | upstream_gene_variant | MODIFIER | c.-2699G>A| |
S221 |
3 | BAA08g08960 | A08 | 8182091 | G | A | upstream_gene_variant | MODIFIER | c.-2673G>A| |
S247 |
4 | BAA08g08960 | A08 | 8182834 | G | A | upstream_gene_variant | MODIFIER | c.-1930G>A| |
S288 |
5 | BAA08g08960 | A08 | 8183713 | G | A | upstream_gene_variant | MODIFIER | c.-1051G>A| |
S107 |
6 | BAA08g08960 | A08 | 8184788 | G | A | missense_variant | MODERATE | c.25G>A|p.Val9Ile |
S190 |
7 | BAA08g08960 | A08 | 8185066 | C | T | missense_variant | MODERATE | c.218C>T|p.Ser73Phe |
S114 |
8 | BAA08g08960 | A08 | 8185707 | G | A | intron_variant | MODIFIER | c.675+17G>A| |
S131 |
9 | BAA08g08960 | A08 | 8186240 | C | T | splice_region_variant&intron_variant | LOW | c.901-6C>T| |
S223 |
10 | BAA08g08960 | A08 | 8186747 | C | T | missense_variant | MODERATE | c.1232C>T|p.Ala411Val |
S183 S198 |
11 | BAA08g08960 | A08 | 8187781 | C | T | synonymous_variant | LOW | c.1843C>T|p.Leu615Leu |
S76 |
12 | BAA08g08960 | A08 | 8190098 | G | A | downstream_gene_variant | MODIFIER | c.*2069G>A| |
S236 |
13 | BAA08g08960 | A08 | 8192116 | C | T | downstream_gene_variant | MODIFIER | c.*4087C>T| |
S143 |
14 | BAA08g08960 | A08 | 8192318 | C | T | downstream_gene_variant | MODIFIER | c.*4289C>T| |
S189 |
15 | BAA08g08960 | A08 | 8192989 | C | T | downstream_gene_variant | MODIFIER | c.*4960C>T| |
S261 |