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
90501 BAA10g00570 A10 286430 C T missense_variant MODERATE c.727C>T|p.Pro243Ser S117
90502 BAA10g00580 A10 287436 C T upstream_gene_variant MODIFIER c.-199C>T| S162
90503 BAA10g00580 A10 287764 G A missense_variant MODERATE c.130G>A|p.Gly44Arg S234
90504 BAA10g00580 A10 287783 G C missense_variant MODERATE c.149G>C|p.Ser50Thr S109
90505 BAA10g00580 A10 287840 C T missense_variant MODERATE c.206C>T|p.Pro69Leu S43
90506 BAA10g00580 A10 287982 C T synonymous_variant LOW c.348C>T|p.Val116Val S67
90507 BAA10g00580 A10 288701 C T missense_variant MODERATE c.1067C>T|p.Thr356Ile S139
90508 BAA10g00590 A10 289289 C T upstream_gene_variant MODIFIER c.-1330C>T| S230
90509 BAA10g00570 A10 290735 G A downstream_gene_variant MODIFIER c.*4159G>A| S1
90510 BAA10g00590 A10 291078 C T synonymous_variant LOW c.270C>T|p.Phe90Phe S270
90511 BAA10g00570 A10 291263 G A downstream_gene_variant MODIFIER c.*4687G>A| S267
90512 BAA10g00600 A10 291791 C T missense_variant MODERATE c.454G>A|p.Asp152Asn S247
90513 BAA10g00600 A10 292077 C T missense_variant MODERATE c.259G>A|p.Ala87Thr S255
90514 BAA10g00600 A10 292108 G A synonymous_variant LOW c.228C>T|p.Leu76Leu S179
90515 BAA10g00600 A10 292406 G A missense_variant MODERATE c.100C>T|p.Leu34Phe S107
90516 BAA10g00600 A10 292514 C T upstream_gene_variant MODIFIER c.-9G>A| S297
90517 BAA10g00600 A10 293409 A G upstream_gene_variant MODIFIER c.-904T>C| S38
90518 BAA10g00600 A10 294271 C T upstream_gene_variant MODIFIER c.-1766G>A| S277
90519 BAA10g00600 A10 294913 C T upstream_gene_variant MODIFIER c.-2408G>A| S181
90520 BAA10g00610 A10 295560 C T missense_variant MODERATE c.766G>A|p.Asp256Asn S188
90521 BAA10g00610 A10 295813 G A synonymous_variant LOW c.513C>T|p.Ile171Ile S5
90522 BAA10g00610 A10 297522 C T upstream_gene_variant MODIFIER c.-1099G>A| S166
90523 BAA10g00610 A10 299104 C T upstream_gene_variant MODIFIER c.-2681G>A| S54
90524 BAA10g00610 A10 300451 G A upstream_gene_variant MODIFIER c.-4028C>T| S80
90525 BAA10g00620 A10 302035 C T synonymous_variant LOW c.1389C>T|p.Val463Val S77
S82