Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4951 | BAA01g04050 | A01 | 1832620 | G | A | upstream_gene_variant | MODIFIER | c.-4701C>T| |
S235 |
4952 | BAA01g04060 | A01 | 1833217 | C | T | synonymous_variant | LOW | c.103C>T|p.Leu35Leu |
S77 |
4953 | BAA01g04060 | A01 | 1833474 | C | T | synonymous_variant | LOW | c.360C>T|p.Gly120Gly |
S299 |
4954 | BAA01g04060 | A01 | 1833589 | G | A | missense_variant | MODERATE | c.475G>A|p.Val159Ile |
S294 |
4955 | BAA01g04070 | A01 | 1834034 | G | A | upstream_gene_variant | MODIFIER | c.-2324G>A| |
S301 S304 |
4956 | BAA01g04070 | A01 | 1834463 | C | T | upstream_gene_variant | MODIFIER | c.-1895C>T| |
S64 |
4957 | BAA01g04070 | A01 | 1834497 | C | T | upstream_gene_variant | MODIFIER | c.-1861C>T| |
S223 |
4958 | BAA01g04060 | A01 | 1835227 | G | A | missense_variant | MODERATE | c.1001G>A|p.Gly334Asp |
S20 |
4959 | BAA01g04070 | A01 | 1835313 | G | A | upstream_gene_variant | MODIFIER | c.-1045G>A| |
S216 |
4960 | BAA01g04070 | A01 | 1835773 | G | A | upstream_gene_variant | MODIFIER | c.-585G>A| |
S294 |
4961 | BAA01g04080 | A01 | 1836942 | C | T | upstream_gene_variant | MODIFIER | c.-3270C>T| |
S207 |
4962 | BAA01g04080 | A01 | 1837399 | C | T | upstream_gene_variant | MODIFIER | c.-2813C>T| |
S176 |
4963 | BAA01g04070 | A01 | 1838169 | G | A | missense_variant | MODERATE | c.1061G>A|p.Gly354Asp |
S142 |
4964 | BAA01g04070 | A01 | 1838203 | G | A | splice_region_variant&intron_variant | LOW | c.1090+5G>A| |
S236 |
4965 | BAA01g04080 | A01 | 1838507 | C | T | upstream_gene_variant | MODIFIER | c.-1705C>T| |
S139 |
4966 | BAA01g04080 | A01 | 1839239 | G | A | upstream_gene_variant | MODIFIER | c.-973G>A| |
S156 |
4967 | BAA01g04080 | A01 | 1839940 | G | A | upstream_gene_variant | MODIFIER | c.-272G>A| |
S172 S217 |
4968 | BAA01g04080 | A01 | 1840492 | G | A | missense_variant | MODERATE | c.181G>A|p.Asp61Asn |
S162 |
4969 | BAA01g04080 | A01 | 1840861 | G | A | missense_variant | MODERATE | c.448G>A|p.Gly150Arg |
S17 |
4970 | BAA01g04080 | A01 | 1841043 | G | A | synonymous_variant | LOW | c.630G>A|p.Thr210Thr |
S257 |
4971 | BAA01g04090 | A01 | 1841542 | G | A | upstream_gene_variant | MODIFIER | c.-2497G>A| |
S169 |
4972 | BAA01g04090 | A01 | 1841590 | C | T | upstream_gene_variant | MODIFIER | c.-2449C>T| |
S120 |
4973 | BAA01g04080 | A01 | 1843231 | C | T | synonymous_variant | LOW | c.1498C>T|p.Leu500Leu |
S61 |
4974 | BAA01g04090 | A01 | 1843563 | G | A | upstream_gene_variant | MODIFIER | c.-476G>A| |
S165 |
4975 | BAA01g04090 | A01 | 1844909 | G | A | missense_variant | MODERATE | c.214G>A|p.Asp72Asn |
S119 |