Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g37000 | A03 | 17044727 | C | T | missense_variant | MODERATE | c.3314G>A|p.Gly1105Glu |
S44 |
2 | BAA03g37000 | A03 | 17044832 | C | T | missense_variant | MODERATE | c.3209G>A|p.Gly1070Glu |
S136 |
3 | BAA03g37000 | A03 | 17045554 | G | A | missense_variant | MODERATE | c.2689C>T|p.Leu897Phe |
S257 |
4 | BAA03g37000 | A03 | 17046134 | C | T | missense_variant | MODERATE | c.2234G>A|p.Ser745Asn |
S66 |
5 | BAA03g37000 | A03 | 17046212 | G | A | missense_variant | MODERATE | c.2156C>T|p.Ser719Phe |
S206 S26 |
6 | BAA03g37000 | A03 | 17046279 | C | T | missense_variant | MODERATE | c.2089G>A|p.Asp697Asn |
S35 |
7 | BAA03g37000 | A03 | 17047196 | C | T | missense_variant | MODERATE | c.1568G>A|p.Arg523Lys |
S173 |
8 | BAA03g37000 | A03 | 17047384 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1381-1G>A| |
S105 S106 |
9 | BAA03g37000 | A03 | 17048863 | C | T | missense_variant | MODERATE | c.1034G>A|p.Arg345Lys |
S298 |
10 | BAA03g37000 | A03 | 17052832 | T | G | upstream_gene_variant | MODIFIER | c.-2035A>C| |
S264 |
11 | BAA03g37000 | A03 | 17053164 | G | A | upstream_gene_variant | MODIFIER | c.-2367C>T| |
S219 S72 |
12 | BAA03g37000 | A03 | 17053252 | G | A | upstream_gene_variant | MODIFIER | c.-2455C>T| |
S162 |
13 | BAA03g37000 | A03 | 17055369 | G | A | upstream_gene_variant | MODIFIER | c.-4572C>T| |
S111 S89 |
14 | BAA03g37000 | A03 | 17055421 | C | T | upstream_gene_variant | MODIFIER | c.-4624G>A| |
S199 |
15 | BAA03g37000 | A03 | 17055443 | C | T | upstream_gene_variant | MODIFIER | c.-4646G>A| |
S4 |
16 | BAA03g37000 | A03 | 17055602 | C | T | upstream_gene_variant | MODIFIER | c.-4805G>A| |
S74 |
17 | BAA03g37000 | A03 | 17055679 | G | A | upstream_gene_variant | MODIFIER | c.-4882C>T| |
S39 |