Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
2051 | BAA01g01660 | A01 | 737155 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S234 |
2052 | BAA01g01660 | A01 | 737471 | G | A | upstream_gene_variant | MODIFIER | c.-2474C>T| |
S256 |
2053 | BAA01g01670 | A01 | 738485 | C | T | missense_variant | MODERATE | c.1301G>A|p.Gly434Asp |
S236 |
2054 | BAA01g01670 | A01 | 739106 | G | A | missense_variant | MODERATE | c.680C>T|p.Ser227Phe |
S289 S290 |
2055 | BAA01g01670 | A01 | 739390 | C | T | synonymous_variant | LOW | c.396G>A|p.Ala132Ala |
S62 |
2056 | BAA01g01670 | A01 | 739594 | G | A | synonymous_variant | LOW | c.192C>T|p.Tyr64Tyr |
S103 |
2057 | BAA01g01670 | A01 | 740173 | C | T | upstream_gene_variant | MODIFIER | c.-388G>A| |
S13 S140 S168 S279 S64 |
2058 | BAA01g01670 | A01 | 740941 | G | A | upstream_gene_variant | MODIFIER | c.-1156C>T| |
S295 |
2059 | BAA01g01670 | A01 | 741747 | C | T | upstream_gene_variant | MODIFIER | c.-1962G>A| |
S252 |
2060 | BAA01g01680 | A01 | 742534 | G | A | missense_variant | MODERATE | c.1280C>T|p.Thr427Met |
S138 |
2061 | BAA01g01680 | A01 | 742710 | C | T | synonymous_variant | LOW | c.1104G>A|p.Thr368Thr |
S53 |
2062 | BAA01g01680 | A01 | 742776 | G | A | synonymous_variant | LOW | c.1038C>T|p.Leu346Leu |
S276 |
2063 | BAA01g01680 | A01 | 743620 | C | T | missense_variant | MODERATE | c.442G>A|p.Glu148Lys |
S139 |
2064 | BAA01g01680 | A01 | 743687 | G | A | synonymous_variant | LOW | c.375C>T|p.Leu125Leu |
S308 |
2065 | BAA01g01680 | A01 | 744049 | C | T | missense_variant | MODERATE | c.13G>A|p.Val5Met |
S277 |
2066 | BAA01g01670 | A01 | 744365 | G | A | upstream_gene_variant | MODIFIER | c.-4580C>T| |
S34 |
2067 | BAA01g01680 | A01 | 747343 | C | T | upstream_gene_variant | MODIFIER | c.-3282G>A| |
S155 S211 |
2068 | BAA01g01680 | A01 | 748187 | C | T | upstream_gene_variant | MODIFIER | c.-4126G>A| |
S164 |
2069 | BAA01g01690 | A01 | 750157 | G | A | missense_variant | MODERATE | c.1192C>T|p.Pro398Ser |
S98 |
2070 | BAA01g01690 | A01 | 750818 | G | A | intron_variant | MODIFIER | c.876+243C>T| |
S112 |
2071 | BAA01g01690 | A01 | 751552 | G | T | missense_variant | MODERATE | c.385C>A|p.Arg129Ser |
S15 S156 S2 S3 S4 S6 |
2072 | BAA01g01690 | A01 | 751859 | C | T | synonymous_variant | LOW | c.78G>A|p.Thr26Thr |
S65 |
2073 | BAA01g01690 | A01 | 753581 | G | A | upstream_gene_variant | MODIFIER | c.-1645C>T| |
S5 |
2074 | BAA01g01690 | A01 | 755099 | C | T | upstream_gene_variant | MODIFIER | c.-3163G>A| |
S134 |
2075 | BAA01g01700 | A01 | 757943 | C | T | downstream_gene_variant | MODIFIER | c.*1661G>A| |
S171 |