Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23850 | A09 | 15194830 | G | A | missense_variant | MODERATE | c.2542C>T|p.Pro848Ser |
S245 |
2 | BAA09g23850 | A09 | 15195098 | G | A | synonymous_variant | LOW | c.2274C>T|p.Ser758Ser |
S157 S163 |
3 | BAA09g23850 | A09 | 15195376 | C | T | missense_variant | MODERATE | c.1996G>A|p.Glu666Lys |
S171 |
4 | BAA09g23850 | A09 | 15196044 | C | T | synonymous_variant | LOW | c.1830G>A|p.Arg610Arg |
S2 |
5 | BAA09g23850 | A09 | 15196093 | C | T | missense_variant | MODERATE | c.1781G>A|p.Arg594His |
S275 |
6 | BAA09g23850 | A09 | 15196915 | C | T | missense_variant | MODERATE | c.1297G>A|p.Val433Met |
S293 |
7 | BAA09g23850 | A09 | 15197189 | G | A | missense_variant | MODERATE | c.1106C>T|p.Ala369Val |
S165 |
8 | BAA09g23850 | A09 | 15197968 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.590-1G>A| |
S113 |
9 | BAA09g23850 | A09 | 15198379 | G | A | synonymous_variant | LOW | c.384C>T|p.Tyr128Tyr |
S176 |
10 | BAA09g23850 | A09 | 15198573 | C | T | missense_variant | MODERATE | c.286G>A|p.Glu96Lys |
S134 |
11 | BAA09g23850 | A09 | 15198771 | G | A | synonymous_variant | LOW | c.234C>T|p.Arg78Arg |
S157 S163 |
12 | BAA09g23850 | A09 | 15199450 | C | T | synonymous_variant | LOW | c.24G>A|p.Lys8Lys |
S296 |
13 | BAA09g23850 | A09 | 15200534 | G | A | upstream_gene_variant | MODIFIER | c.-1061C>T| |
S1 S90 |
14 | BAA09g23850 | A09 | 15201065 | C | T | upstream_gene_variant | MODIFIER | c.-1592G>A| |
S270 S91 |
15 | BAA09g23850 | A09 | 15201886 | G | A | upstream_gene_variant | MODIFIER | c.-2413C>T| |
S74 |
16 | BAA09g23850 | A09 | 15202086 | G | A | upstream_gene_variant | MODIFIER | c.-2613C>T| |
S155 S211 |