Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
166551 BAA02g12600 A02 5647452 C T upstream_gene_variant MODIFIER c.-3714G>A| S185
166552 BAA02g12610 A02 5647838 G A missense_variant MODERATE c.395C>T|p.Pro132Leu S289
S290
166553 BAA02g12610 A02 5649302 G A upstream_gene_variant MODIFIER c.-702C>T| S184
166554 BAA02g12610 A02 5649731 G A upstream_gene_variant MODIFIER c.-1131C>T| S122
166555 BAA02g12610 A02 5650415 C T upstream_gene_variant MODIFIER c.-1815G>A| S112
166556 BAA02g12610 A02 5650620 C T upstream_gene_variant MODIFIER c.-2020G>A| S99
166557 BAA02g12620 A02 5651022 G A synonymous_variant LOW c.306C>T|p.Tyr102Tyr S158
166558 BAA02g12620 A02 5651210 G A synonymous_variant LOW c.216C>T|p.Asn72Asn S298
166559 BAA02g12620 A02 5651335 G A stop_gained HIGH c.175C>T|p.Gln59* S133
166560 BAA02g12610 A02 5651609 G A upstream_gene_variant MODIFIER c.-3009C>T| S23
166561 BAA02g12630 A02 5653168 G A missense_variant MODERATE c.526G>A|p.Ala176Thr S269
166562 BAA02g12630 A02 5653299 G A synonymous_variant LOW c.657G>A|p.Lys219Lys S156
166563 BAA02g12630 A02 5653368 G A synonymous_variant LOW c.726G>A|p.Glu242Glu S67
166564 BAA02g12630 A02 5653522 G A missense_variant MODERATE c.880G>A|p.Gly294Ser S37
166565 BAA02g12630 A02 5653828 C T missense_variant MODERATE c.1102C>T|p.Pro368Ser S212
166566 BAA02g12630 A02 5653874 C T missense_variant MODERATE c.1148C>T|p.Ala383Val S216
166567 BAA02g12630 A02 5654390 C T synonymous_variant LOW c.1513C>T|p.Leu505Leu S115
166568 BAA02g12630 A02 5654682 C T missense_variant MODERATE c.1805C>T|p.Ser602Phe S219
S72
166569 BAA02g12630 A02 5654694 C T missense_variant MODERATE c.1817C>T|p.Ser606Phe S87
166570 BAA02g12630 A02 5654756 C T missense_variant MODERATE c.1879C>T|p.Leu627Phe S159
S188
S243
S276
S298
S299
166571 BAA02g12630 A02 5655027 C T synonymous_variant LOW c.2070C>T|p.Asn690Asn S78
S83
166572 BAA02g12620 A02 5655718 C T upstream_gene_variant MODIFIER c.-4209G>A| S78
S83
166573 BAA02g12620 A02 5655903 C T upstream_gene_variant MODIFIER c.-4394G>A| S180
166574 BAA02g12620 A02 5655973 C T upstream_gene_variant MODIFIER c.-4464G>A| S152
166575 BAA02g12640 A02 5656242 G A missense_variant MODERATE c.3983C>T|p.Pro1328Leu S271