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
141101 BAA10g26150 A10 20854257 T A upstream_gene_variant MODIFIER c.-4711T>A| S257
141102 BAA10g26150 A10 20854286 G A upstream_gene_variant MODIFIER c.-4682G>A| S262
141103 BAA10g26150 A10 20854528 G A upstream_gene_variant MODIFIER c.-4440G>A| S267
141104 BAA10g26150 A10 20856424 G T upstream_gene_variant MODIFIER c.-2544G>T| S156
141105 BAA10g26150 A10 20856543 G A upstream_gene_variant MODIFIER c.-2425G>A| S190
141106 BAA10g26150 A10 20857547 G A upstream_gene_variant MODIFIER c.-1421G>A| S219
S72
141107 BAA10g26150 A10 20857809 C T upstream_gene_variant MODIFIER c.-1159C>T| S275
141108 BAA10g26150 A10 20857980 G A upstream_gene_variant MODIFIER c.-988G>A| S179
141109 BAA10g26150 A10 20858267 C T upstream_gene_variant MODIFIER c.-701C>T| S18
141110 BAA10g26150 A10 20858689 C T upstream_gene_variant MODIFIER c.-279C>T| S38
141111 BAA10g26150 A10 20860597 G A missense_variant MODERATE c.647G>A|p.Arg216Lys S59
141112 BAA10g26150 A10 20860829 C T synonymous_variant LOW c.879C>T|p.Ala293Ala S195
141113 BAA10g26170 A10 20861387 C T upstream_gene_variant MODIFIER c.-4512C>T| S296
141114 BAA10g26170 A10 20861666 C T upstream_gene_variant MODIFIER c.-4233C>T| S281
141115 BAA10g26160 A10 20862439 C T missense_variant MODERATE c.1187G>A|p.Gly396Glu S196
141116 BAA10g26160 A10 20862599 G A stop_gained HIGH c.1027C>T|p.Gln343* S269
141117 BAA10g26170 A10 20863700 G A upstream_gene_variant MODIFIER c.-2199G>A| S1
S90
141118 BAA10g26160 A10 20863974 G A missense_variant MODERATE c.136C>T|p.Leu46Phe S80
141119 BAA10g26170 A10 20864182 C T upstream_gene_variant MODIFIER c.-1717C>T| S166
141120 BAA10g26160 A10 20865404 G A upstream_gene_variant MODIFIER c.-974C>T| S303
141121 BAA10g26170 A10 20866485 C T missense_variant MODERATE c.587C>T|p.Pro196Leu S200
141122 BAA10g26170 A10 20866519 G A synonymous_variant LOW c.621G>A|p.Lys207Lys S233
141123 BAA10g26170 A10 20866543 C T synonymous_variant LOW c.645C>T|p.Ser215Ser S144
141124 BAA10g26170 A10 20866646 G A missense_variant MODERATE c.748G>A|p.Asp250Asn S303
141125 BAA10g26170 A10 20866666 G A stop_gained HIGH c.768G>A|p.Trp256* S75
S81