Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g32630 | A10 | 23393453 | C | T | synonymous_variant | LOW | c.2247G>A|p.Lys749Lys |
S61 |
2 | BAA10g32630 | A10 | 23393589 | C | T | synonymous_variant | LOW | c.2184G>A|p.Leu728Leu |
S206 S26 |
3 | BAA10g32630 | A10 | 23393607 | G | A | synonymous_variant | LOW | c.2166C>T|p.Ser722Ser |
S172 S217 |
4 | BAA10g32630 | A10 | 23393756 | C | T | missense_variant | MODERATE | c.2017G>A|p.Glu673Lys |
S195 |
5 | BAA10g32630 | A10 | 23394213 | G | A | synonymous_variant | LOW | c.1878C>T|p.Gly626Gly |
S255 |
6 | BAA10g32630 | A10 | 23394346 | G | A | missense_variant | MODERATE | c.1745C>T|p.Thr582Met |
S166 |
7 | BAA10g32630 | A10 | 23394455 | C | T | missense_variant | MODERATE | c.1636G>A|p.Asp546Asn |
S103 |
8 | BAA10g32630 | A10 | 23395071 | C | T | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S10 |
9 | BAA10g32630 | A10 | 23395455 | G | A | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S79 S84 |
10 | BAA10g32630 | A10 | 23395835 | G | A | synonymous_variant | LOW | c.838C>T|p.Leu280Leu |
S35 |
11 | BAA10g32630 | A10 | 23397059 | C | T | upstream_gene_variant | MODIFIER | c.-387G>A| |
S34 |
12 | BAA10g32630 | A10 | 23397839 | C | T | upstream_gene_variant | MODIFIER | c.-1167G>A| |
S161 |
13 | BAA10g32630 | A10 | 23399114 | C | T | upstream_gene_variant | MODIFIER | c.-2442G>A| |
S144 |