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
92201 BAA10g01980 A10 952190 G A downstream_gene_variant MODIFIER c.*3018G>A| S80
92202 BAA10g01980 A10 952561 C T downstream_gene_variant MODIFIER c.*3389C>T| S23
92203 BAA10g01980 A10 952937 G A downstream_gene_variant MODIFIER c.*3765G>A| S48
92204 BAA10g01980 A10 953143 G A downstream_gene_variant MODIFIER c.*3971G>A| S4
92205 BAA10g01980 A10 953176 C T downstream_gene_variant MODIFIER c.*4004C>T| S87
92206 BAA10g01980 A10 953773 G A downstream_gene_variant MODIFIER c.*4601G>A| S189
92207 BAA10g01990 A10 954294 G A downstream_gene_variant MODIFIER c.*119C>T| S97
92208 BAA10g01990 A10 954495 G A intron_variant MODIFIER c.3386-72C>T| S13
92209 BAA10g01990 A10 954574 G A intron_variant MODIFIER c.3386-151C>T| S69
92210 BAA10g01990 A10 954998 G A intron_variant MODIFIER c.3385+447C>T| S76
92211 BAA10g01990 A10 955143 G A intron_variant MODIFIER c.3385+302C>T| S293
92212 BAA10g01990 A10 956645 C T missense_variant MODERATE c.2248G>A|p.Glu750Lys S287
92213 BAA10g01990 A10 956691 C T synonymous_variant LOW c.2202G>A|p.Lys734Lys S139
92214 BAA10g01990 A10 957061 C T missense_variant MODERATE c.1832G>A|p.Ser611Asn S197
92215 BAA10g01990 A10 958003 C T missense_variant MODERATE c.890G>A|p.Arg297Lys S114
92216 BAA10g01990 A10 959782 G A upstream_gene_variant MODIFIER c.-477C>T| S219
S72
92217 BAA10g01990 A10 960436 G A upstream_gene_variant MODIFIER c.-1131C>T| S215
92218 BAA10g01990 A10 960768 C T upstream_gene_variant MODIFIER c.-1463G>A| S149
92219 BAA10g01990 A10 961130 C T upstream_gene_variant MODIFIER c.-1825G>A| S171
92220 BAA10g02000 A10 961560 G A missense_variant MODERATE c.280G>A|p.Val94Ile S203
92221 BAA10g02000 A10 961762 G A missense_variant MODERATE c.394G>A|p.Glu132Lys S234
92222 BAA10g01990 A10 962361 C T upstream_gene_variant MODIFIER c.-3056G>A| S294
92223 BAA10g02010 A10 962523 G A missense_variant MODERATE c.73G>A|p.Asp25Asn S55
92224 BAA10g02010 A10 962605 C T missense_variant MODERATE c.155C>T|p.Ser52Phe S287
92225 BAA10g02010 A10 963013 G A missense_variant MODERATE c.563G>A|p.Gly188Glu S112