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
146151 BAA10g30590 A10 22632857 G A upstream_gene_variant MODIFIER c.-1947G>A| S303
146152 BAA10g30580 A10 22633324 G A synonymous_variant LOW c.759G>A|p.Gln253Gln S46
146153 BAA10g30580 A10 22633730 G A missense_variant MODERATE c.1165G>A|p.Gly389Arg S209
146154 BAA10g30580 A10 22634012 G A synonymous_variant LOW c.1380G>A|p.Gln460Gln S1
S90
146155 BAA10g30590 A10 22634959 G A synonymous_variant LOW c.156G>A|p.Arg52Arg S216
146156 BAA10g30600 A10 22635992 G A missense_variant MODERATE c.968C>T|p.Ala323Val S116
146157 BAA10g30600 A10 22636429 G A missense_variant MODERATE c.620C>T|p.Thr207Ile S134
146158 BAA10g30600 A10 22636752 C T synonymous_variant LOW c.372G>A|p.Lys124Lys S87
146159 BAA10g30610 A10 22639845 C T missense_variant MODERATE c.917C>T|p.Pro306Leu S63
146160 BAA10g30610 A10 22639899 G A missense_variant MODERATE c.971G>A|p.Gly324Glu S176
146161 BAA10g30610 A10 22639903 C T synonymous_variant LOW c.975C>T|p.Phe325Phe S295
146162 BAA10g30610 A10 22640434 C T synonymous_variant LOW c.1506C>T|p.Gly502Gly S225
146163 BAA10g30610 A10 22640629 G A stop_gained HIGH c.1701G>A|p.Trp567* S223
146164 BAA10g30610 A10 22641067 C T synonymous_variant LOW c.2139C>T|p.Leu713Leu S204
146165 BAA10g30600 A10 22641687 G A upstream_gene_variant MODIFIER c.-4138C>T| S262
146166 BAA10g30620 A10 22641905 C T missense_variant MODERATE c.1972G>A|p.Ala658Thr S236
146167 BAA10g30620 A10 22642380 C T missense_variant MODERATE c.1648G>A|p.Asp550Asn S130
146168 BAA10g30620 A10 22642841 C T missense_variant MODERATE c.1321G>A|p.Ala441Thr S260
146169 BAA10g30620 A10 22644092 G A missense_variant MODERATE c.212C>T|p.Ser71Phe S158
146170 BAA10g30630 A10 22647266 G A synonymous_variant LOW c.171C>T|p.Cys57Cys S125
146171 BAA10g30620 A10 22647585 G A upstream_gene_variant MODIFIER c.-3282C>T| S54
146172 BAA10g30640 A10 22647829 G A synonymous_variant LOW c.904C>T|p.Leu302Leu S167
146173 BAA10g30640 A10 22648498 G A missense_variant MODERATE c.385C>T|p.Leu129Phe S261
146174 BAA10g30640 A10 22648649 G A synonymous_variant LOW c.234C>T|p.Ile78Ile S88
146175 BAA10g30630 A10 22649995 C T upstream_gene_variant MODIFIER c.-2559G>A| S12