Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
4201 | BAA01g03420 | A01 | 1551815 | G | A | missense_variant | MODERATE | c.1306G>A|p.Glu436Lys |
S204 |
4202 | BAA01g03420 | A01 | 1551839 | G | A | missense_variant | MODERATE | c.1330G>A|p.Gly444Arg |
S308 |
4203 | BAA01g03420 | A01 | 1552232 | G | A | missense_variant | MODERATE | c.1580G>A|p.Arg527Lys |
S32 |
4204 | BAA01g03420 | A01 | 1552301 | G | A | missense_variant | MODERATE | c.1649G>A|p.Arg550Lys |
S7 |
4205 | BAA01g03420 | A01 | 1552997 | C | T | missense_variant | MODERATE | c.2140C>T|p.Arg714Cys |
S50 |
4206 | BAA01g03420 | A01 | 1553049 | C | T | missense_variant | MODERATE | c.2192C>T|p.Thr731Met |
S107 |
4207 | BAA01g03420 | A01 | 1553166 | G | A | missense_variant | MODERATE | c.2309G>A|p.Gly770Asp |
S247 |
4208 | BAA01g03430 | A01 | 1553821 | C | T | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S182 |
4209 | BAA01g03430 | A01 | 1554176 | C | T | upstream_gene_variant | MODIFIER | c.-1343C>T| |
S125 |
4210 | BAA01g03430 | A01 | 1554227 | G | A | upstream_gene_variant | MODIFIER | c.-1292G>A| |
S297 |
4211 | BAA01g03430 | A01 | 1555119 | G | A | upstream_gene_variant | MODIFIER | c.-400G>A| |
S7 |
4212 | BAA01g03450 | A01 | 1556179 | C | T | upstream_gene_variant | MODIFIER | c.-3601C>T| |
S231 |
4213 | BAA01g03430 | A01 | 1556994 | G | A | synonymous_variant | LOW | c.885G>A|p.Thr295Thr |
S166 |
4214 | BAA01g03450 | A01 | 1557453 | G | A | upstream_gene_variant | MODIFIER | c.-2327G>A| |
S276 |
4215 | BAA01g03430 | A01 | 1558024 | G | A | synonymous_variant | LOW | c.1245G>A|p.Glu415Glu |
S5 |
4216 | BAA01g03450 | A01 | 1558804 | C | T | upstream_gene_variant | MODIFIER | c.-976C>T| |
S41 |
4217 | BAA01g03440 | A01 | 1560975 | G | A | upstream_gene_variant | MODIFIER | c.-1783C>T| |
S73 S91 |
4218 | BAA01g03450 | A01 | 1562127 | C | T | synonymous_variant | LOW | c.1107C>T|p.Phe369Phe |
S187 |
4219 | BAA01g03450 | A01 | 1562210 | G | A | missense_variant | MODERATE | c.1190G>A|p.Gly397Glu |
S73 S91 |
4220 | BAA01g03450 | A01 | 1562254 | C | T | missense_variant | MODERATE | c.1234C>T|p.Leu412Phe |
S2 |
4221 | BAA01g03450 | A01 | 1562455 | G | A | missense_variant | MODERATE | c.1357G>A|p.Asp453Asn |
S217 |
4222 | BAA01g03450 | A01 | 1562773 | C | T | synonymous_variant | LOW | c.1590C>T|p.Ser530Ser |
S155 S211 |
4223 | BAA01g03450 | A01 | 1563354 | C | T | synonymous_variant | LOW | c.1908C>T|p.Leu636Leu |
S266 |
4224 | BAA01g03450 | A01 | 1563462 | G | A | stop_gained | HIGH | c.2016G>A|p.Trp672* |
S217 |
4225 | BAA01g03470 | A01 | 1564722 | C | T | upstream_gene_variant | MODIFIER | c.-3219C>T| |
S265 |