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
122001 BAA10g12570 A10 13969649 C T upstream_gene_variant MODIFIER c.-4961G>A| S177
122002 BAA10g12580 A10 13970027 G A downstream_gene_variant MODIFIER c.*3662C>T| S288
122003 BAA10g12580 A10 13971261 G A downstream_gene_variant MODIFIER c.*2428C>T| S186
122004 BAA10g12580 A10 13971767 G A downstream_gene_variant MODIFIER c.*1922C>T| S15
122005 BAA10g12580 A10 13973030 C T downstream_gene_variant MODIFIER c.*659G>A| S162
122006 BAA10g12580 A10 13973965 G A intron_variant MODIFIER c.1974-24C>T| S34
122007 BAA10g12580 A10 13974646 C T missense_variant MODERATE c.1429G>A|p.Gly477Ser S74
122008 BAA10g12580 A10 13974666 C T missense_variant MODERATE c.1409G>A|p.Arg470Gln S281
122009 BAA10g12580 A10 13974888 G A missense_variant MODERATE c.1187C>T|p.Ser396Phe S284
122010 BAA10g12580 A10 13974984 G A missense_variant MODERATE c.1091C>T|p.Ser364Phe S159
S187
S188
S243
S276
122011 BAA10g12580 A10 13975069 C T missense_variant MODERATE c.1006G>A|p.Asp336Asn S238
122012 BAA10g12580 A10 13975500 C T intron_variant MODIFIER c.610-35G>A| S45
122013 BAA10g12580 A10 13976073 G A intron_variant MODIFIER c.181-107C>T| S212
122014 BAA10g12580 A10 13977415 G A upstream_gene_variant MODIFIER c.-878C>T| S303
122015 BAA10g12580 A10 13978891 C T upstream_gene_variant MODIFIER c.-2354G>A| S133
122016 BAA10g12580 A10 13979240 G A upstream_gene_variant MODIFIER c.-2703C>T| S125
122017 BAA10g12580 A10 13979465 G T upstream_gene_variant MODIFIER c.-2928C>A| S279
122018 BAA10g12580 A10 13979809 C T upstream_gene_variant MODIFIER c.-3272G>A| S152
122019 BAA10g12580 A10 13979923 C T upstream_gene_variant MODIFIER c.-3386G>A| S180
122020 BAA10g12580 A10 13981143 G A upstream_gene_variant MODIFIER c.-4606C>T| S151
S263
122021 BAA10g12580 A10 13981496 G A upstream_gene_variant MODIFIER c.-4959C>T| S295
122022 BAA10g12590 A10 13983395 C T splice_region_variant&stop_retained_variant LOW c.1259G>A|p.Ter420Ter S37
122023 BAA10g12590 A10 13983962 G A missense_variant MODERATE c.874C>T|p.Leu292Phe S230
122024 BAA10g12600 A10 13985544 C T upstream_gene_variant MODIFIER c.-3308C>T| S236
122025 BAA10g12590 A10 13985761 C T synonymous_variant LOW c.513G>A|p.Lys171Lys S122