Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g32880 | A08 | 21562749 | C | T | upstream_gene_variant | MODIFIER | c.-4432C>T| |
S197 |
2 | BAA08g32880 | A08 | 21564152 | G | A | upstream_gene_variant | MODIFIER | c.-3029G>A| |
S182 |
3 | BAA08g32880 | A08 | 21564182 | G | A | upstream_gene_variant | MODIFIER | c.-2999G>A| |
S12 S23 |
4 | BAA08g32880 | A08 | 21565070 | G | A | upstream_gene_variant | MODIFIER | c.-2111G>A| |
S272 |
5 | BAA08g32880 | A08 | 21565356 | G | A | upstream_gene_variant | MODIFIER | c.-1825G>A| |
S72 |
6 | BAA08g32880 | A08 | 21565674 | A | G | upstream_gene_variant | MODIFIER | c.-1507A>G| |
S6 |
7 | BAA08g32880 | A08 | 21565711 | C | T | upstream_gene_variant | MODIFIER | c.-1470C>T| |
S278 |
8 | BAA08g32880 | A08 | 21567543 | C | T | missense_variant | MODERATE | c.245C>T|p.Thr82Ile |
S299 |
9 | BAA08g32880 | A08 | 21567563 | C | T | missense_variant | MODERATE | c.265C>T|p.Pro89Ser |
S50 |
10 | BAA08g32880 | A08 | 21568153 | C | T | missense_variant | MODERATE | c.707C>T|p.Ala236Val |
S20 |
11 | BAA08g32880 | A08 | 21568510 | G | A | synonymous_variant | LOW | c.975G>A|p.Ala325Ala |
S206 S26 |
12 | BAA08g32880 | A08 | 21569397 | G | A | missense_variant | MODERATE | c.1757G>A|p.Ser586Asn |
S16 |
13 | BAA08g32880 | A08 | 21571399 | C | T | missense_variant | MODERATE | c.2726C>T|p.Ala909Val |
S143 |