Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g42390 | A07 | 36760339 | C | T | upstream_gene_variant | MODIFIER | c.-1626C>T| |
S261 |
2 | BAA07g42390 | A07 | 36761174 | C | T | upstream_gene_variant | MODIFIER | c.-791C>T| |
S13 |
3 | BAA07g42390 | A07 | 36761338 | C | T | upstream_gene_variant | MODIFIER | c.-627C>T| |
S144 |
4 | BAA07g42390 | A07 | 36761647 | G | A | upstream_gene_variant | MODIFIER | c.-318G>A| |
S287 |
5 | BAA07g42390 | A07 | 36761943 | G | A | upstream_gene_variant | MODIFIER | c.-22G>A| |
S159 |
6 | BAA07g42390 | A07 | 36762185 | C | T | missense_variant | MODERATE | c.106C>T|p.Arg36Trp |
S121 |
7 | BAA07g42390 | A07 | 36762606 | C | T | missense_variant | MODERATE | c.427C>T|p.Pro143Ser |
S185 |
8 | BAA07g42390 | A07 | 36763371 | C | T | missense_variant&splice_region_variant | MODERATE | c.739C>T|p.Pro247Ser |
S201 |
9 | BAA07g42390 | A07 | 36763475 | C | T | synonymous_variant | LOW | c.843C>T|p.Leu281Leu |
S221 |
10 | BAA07g42390 | A07 | 36764055 | C | T | synonymous_variant | LOW | c.1057C>T|p.Leu353Leu |
S224 |
11 | BAA07g42390 | A07 | 36764108 | C | T | synonymous_variant | LOW | c.1110C>T|p.Ile370Ile |
S164 |
12 | BAA07g42390 | A07 | 36764128 | G | A | missense_variant | MODERATE | c.1130G>A|p.Ser377Asn |
S157 |
13 | BAA07g42390 | A07 | 36764179 | C | T | missense_variant | MODERATE | c.1181C>T|p.Ser394Phe |
S53 |
14 | BAA07g42390 | A07 | 36764752 | G | A | missense_variant | MODERATE | c.1605G>A|p.Met535Ile |
S273 |
15 | BAA07g42390 | A07 | 36764756 | G | A | missense_variant | MODERATE | c.1609G>A|p.Gly537Ser |
S84 S93 |
16 | BAA07g42390 | A07 | 36765052 | G | A | missense_variant&splice_region_variant | MODERATE | c.1819G>A|p.Glu607Lys |
S209 |
17 | BAA07g42390 | A07 | 36765205 | G | A | stop_gained | HIGH | c.1896G>A|p.Trp632* |
S276 |
18 | BAA07g42390 | A07 | 36765218 | G | A | missense_variant | MODERATE | c.1909G>A|p.Val637Ile |
S135 |
19 | BAA07g42390 | A07 | 36765425 | G | A | missense_variant | MODERATE | c.2029G>A|p.Ala677Thr |
S65 |
20 | BAA07g42390 | A07 | 36768340 | C | T | downstream_gene_variant | MODIFIER | c.*2348C>T| |
S63 |