Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14000 | A08 | 12028715 | G | A | upstream_gene_variant | MODIFIER | c.-4502G>A| |
S193 |
2 | BAA08g14000 | A08 | 12029843 | A | T | upstream_gene_variant | MODIFIER | c.-3374A>T| |
S68 |
3 | BAA08g14000 | A08 | 12030636 | C | T | upstream_gene_variant | MODIFIER | c.-2581C>T| |
S157 S163 |
4 | BAA08g14000 | A08 | 12030928 | C | T | upstream_gene_variant | MODIFIER | c.-2289C>T| |
S271 |
5 | BAA08g14000 | A08 | 12032166 | G | A | upstream_gene_variant | MODIFIER | c.-1051G>A| |
S128 |
6 | BAA08g14000 | A08 | 12032612 | C | T | upstream_gene_variant | MODIFIER | c.-605C>T| |
S215 |
7 | BAA08g14000 | A08 | 12033503 | G | A | synonymous_variant | LOW | c.102G>A|p.Ser34Ser |
S298 |
8 | BAA08g14000 | A08 | 12035116 | G | A | intron_variant | MODIFIER | c.512+212G>A| |
S151 S261 S263 S274 S303 |
9 | BAA08g14000 | A08 | 12035149 | G | A | intron_variant | MODIFIER | c.512+245G>A| |
S11 |
10 | BAA08g14000 | A08 | 12035188 | C | T | intron_variant | MODIFIER | c.512+284C>T| |
S139 |
11 | BAA08g14000 | A08 | 12038476 | C | T | missense_variant | MODERATE | c.1199C>T|p.Ser400Phe |
S144 |
12 | BAA08g14000 | A08 | 12039209 | G | A | missense_variant&splice_region_variant | MODERATE | c.1615G>A|p.Glu539Lys |
S280 |
13 | BAA08g14000 | A08 | 12039832 | C | T | missense_variant | MODERATE | c.2032C>T|p.Pro678Ser |
S297 |