Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05610 | A07 | 5522778 | A | C | upstream_gene_variant | MODIFIER | c.-1597A>C| |
S217 |
2 | BAA07g05610 | A07 | 5523189 | C | T | upstream_gene_variant | MODIFIER | c.-1186C>T| |
S161 |
3 | BAA07g05610 | A07 | 5524001 | G | A | upstream_gene_variant | MODIFIER | c.-374G>A| |
S239 |
4 | BAA07g05610 | A07 | 5524470 | C | T | synonymous_variant | LOW | c.96C>T|p.Ser32Ser |
S293 |
5 | BAA07g05610 | A07 | 5525392 | C | T | missense_variant | MODERATE | c.1018C>T|p.Pro340Ser |
S168 |
6 | BAA07g05610 | A07 | 5525420 | G | A | missense_variant | MODERATE | c.1046G>A|p.Gly349Glu |
S151 S236 S257 |
7 | BAA07g05610 | A07 | 5525508 | C | T | synonymous_variant | LOW | c.1134C>T|p.Ser378Ser |
S133 |
8 | BAA07g05610 | A07 | 5525661 | G | A | synonymous_variant | LOW | c.1287G>A|p.Arg429Arg |
S83 S88 |
9 | BAA07g05610 | A07 | 5525701 | C | T | stop_gained | HIGH | c.1327C>T|p.Gln443* |
S47 |
10 | BAA07g05610 | A07 | 5525844 | C | T | synonymous_variant | LOW | c.1470C>T|p.Leu490Leu |
S192 |
11 | BAA07g05610 | A07 | 5526227 | C | T | missense_variant | MODERATE | c.1628C>T|p.Ser543Phe |
S198 |
12 | BAA07g05610 | A07 | 5526249 | C | T | synonymous_variant | LOW | c.1650C>T|p.His550His |
S294 |
13 | BAA07g05610 | A07 | 5526302 | G | A | missense_variant | MODERATE | c.1703G>A|p.Arg568Gln |
S54 |
14 | BAA07g05610 | A07 | 5526359 | C | T | missense_variant | MODERATE | c.1760C>T|p.Ser587Phe |
S52 |
15 | BAA07g05610 | A07 | 5526658 | G | A | missense_variant | MODERATE | c.2059G>A|p.Asp687Asn |
S146 |
16 | BAA07g05610 | A07 | 5526694 | C | T | missense_variant | MODERATE | c.2095C>T|p.Pro699Ser |
S32 |
17 | BAA07g05610 | A07 | 5531615 | G | A | downstream_gene_variant | MODIFIER | c.*1013G>A| |
S194 |