Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g50590 | A03 | 24485183 | G | A | missense_variant | MODERATE | c.1358C>T|p.Ser453Phe |
S46 |
2 | BAA03g50590 | A03 | 24485444 | G | A | missense_variant | MODERATE | c.1097C>T|p.Ser366Leu |
S174 |
3 | BAA03g50590 | A03 | 24485473 | T | G | missense_variant | MODERATE | c.1068A>C|p.Glu356Asp |
S139 S15 S150 S156 S189 S207 S215 S223 S229 S252 S259 S273 S284 S308 S38 |
4 | BAA03g50590 | A03 | 24485528 | G | A | missense_variant | MODERATE | c.1013C>T|p.Ser338Phe |
S123 |
5 | BAA03g50590 | A03 | 24485838 | C | T | missense_variant | MODERATE | c.703G>A|p.Ala235Thr |
S2 |
6 | BAA03g50590 | A03 | 24485952 | C | T | missense_variant | MODERATE | c.589G>A|p.Asp197Asn |
S293 |
7 | BAA03g50590 | A03 | 24488943 | G | A | intron_variant | MODIFIER | c.258+1904C>T| |
S152 |
8 | BAA03g50590 | A03 | 24490154 | G | A | intron_variant | MODIFIER | c.258+693C>T| |
S278 |
9 | BAA03g50590 | A03 | 24490760 | G | A | intron_variant | MODIFIER | c.258+87C>T| |
S287 |
10 | BAA03g50590 | A03 | 24492654 | G | A | upstream_gene_variant | MODIFIER | c.-1550C>T| |
S257 |
11 | BAA03g50590 | A03 | 24493170 | C | T | upstream_gene_variant | MODIFIER | c.-2066G>A| |
S157 S163 |
12 | BAA03g50590 | A03 | 24494104 | G | A | upstream_gene_variant | MODIFIER | c.-3000C>T| |
S265 |
13 | BAA03g50590 | A03 | 24494533 | G | A | upstream_gene_variant | MODIFIER | c.-3429C>T| |
S6 |
14 | BAA03g50590 | A03 | 24494654 | G | A | upstream_gene_variant | MODIFIER | c.-3550C>T| |
S84 S93 |
15 | BAA03g50590 | A03 | 24495525 | C | T | upstream_gene_variant | MODIFIER | c.-4421G>A| |
S274 |