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
130351 BAA10g17950 A10 17043396 G A synonymous_variant LOW c.1185G>A|p.Lys395Lys S192
130352 BAA10g17960 A10 17044890 G A missense_variant MODERATE c.152G>A|p.Arg51Lys S289
S290
130353 BAA10g17940 A10 17045580 C T upstream_gene_variant MODIFIER c.-4734G>A| S89
130354 BAA10g17970 A10 17049373 G A upstream_gene_variant MODIFIER c.-2381G>A| S138
130355 BAA10g17970 A10 17049636 G A upstream_gene_variant MODIFIER c.-2118G>A| S97
130356 BAA10g17970 A10 17050924 C T upstream_gene_variant MODIFIER c.-830C>T| S45
130357 BAA10g17970 A10 17053238 G A synonymous_variant LOW c.1020G>A|p.Lys340Lys S267
130358 BAA10g17970 A10 17053918 G A synonymous_variant LOW c.1605G>A|p.Gly535Gly S67
130359 BAA10g17970 A10 17054097 C T missense_variant MODERATE c.1702C>T|p.Pro568Ser S187
130360 BAA10g17980 A10 17054461 C T upstream_gene_variant MODIFIER c.-1236C>T| S20
130361 BAA10g17980 A10 17054701 C T upstream_gene_variant MODIFIER c.-996C>T| S190
130362 BAA10g17980 A10 17054992 C T upstream_gene_variant MODIFIER c.-705C>T| S25
130363 BAA10g17980 A10 17055469 C T upstream_gene_variant MODIFIER c.-228C>T| S275
130364 BAA10g17980 A10 17057036 G A missense_variant MODERATE c.727G>A|p.Asp243Asn S67
130365 BAA10g17980 A10 17057096 C T missense_variant MODERATE c.787C>T|p.Leu263Phe S143
130366 BAA10g17980 A10 17058245 G A missense_variant MODERATE c.1936G>A|p.Gly646Arg S48
130367 BAA10g17970 A10 17058658 T A downstream_gene_variant MODIFIER c.*4247T>A| S273
130368 BAA10g17980 A10 17059926 C T downstream_gene_variant MODIFIER c.*1442C>T| S79
S91
130369 BAA10g17980 A10 17060005 C T downstream_gene_variant MODIFIER c.*1521C>T| S83
130370 BAA10g17990 A10 17060995 G A upstream_gene_variant MODIFIER c.-43C>T| S240
130371 BAA10g17990 A10 17061290 G A upstream_gene_variant MODIFIER c.-338C>T| S138
130372 BAA10g17990 A10 17062156 C T upstream_gene_variant MODIFIER c.-1204G>A| S153
S306
130373 BAA10g17990 A10 17062195 C A upstream_gene_variant MODIFIER c.-1243G>T| S265
130374 BAA10g17990 A10 17062296 C T upstream_gene_variant MODIFIER c.-1344G>A| S148
S210
S30
S31
130375 BAA10g17990 A10 17063030 C T upstream_gene_variant MODIFIER c.-2078G>A| S200