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
141001 BAA10g26100 A10 20811372 C T missense_variant MODERATE c.1532G>A|p.Arg511Lys S224
141002 BAA10g26100 A10 20811998 C T synonymous_variant LOW c.906G>A|p.Gly302Gly S244
141003 BAA10g26100 A10 20814400 T A upstream_gene_variant MODIFIER c.-1497A>T| S157
S163
141004 BAA10g26100 A10 20815371 G A upstream_gene_variant MODIFIER c.-2468C>T| S17
141005 BAA10g26100 A10 20816177 G A upstream_gene_variant MODIFIER c.-3274C>T| S138
141006 BAA10g26100 A10 20816195 C T upstream_gene_variant MODIFIER c.-3292G>A| S268
141007 BAA10g26110 A10 20817905 C T upstream_gene_variant MODIFIER c.-307G>A| S19
141008 BAA10g26110 A10 20817990 C T upstream_gene_variant MODIFIER c.-392G>A| S149
141009 BAA10g26110 A10 20818391 C T upstream_gene_variant MODIFIER c.-793G>A| S185
141010 BAA10g26110 A10 20818603 G A upstream_gene_variant MODIFIER c.-1005C>T| S219
141011 BAA10g26110 A10 20820308 C T upstream_gene_variant MODIFIER c.-2710G>A| S230
141012 BAA10g26110 A10 20820452 C T upstream_gene_variant MODIFIER c.-2854G>A| S246
141013 BAA10g26120 A10 20820964 G A synonymous_variant LOW c.1938C>T|p.Pro646Pro S197
141014 BAA10g26120 A10 20821926 G A missense_variant MODERATE c.976C>T|p.Pro326Ser S127
141015 BAA10g26120 A10 20821936 G A synonymous_variant LOW c.966C>T|p.Arg322Arg S128
141016 BAA10g26120 A10 20822486 G A missense_variant MODERATE c.416C>T|p.Ser139Phe S128
141017 BAA10g26120 A10 20823203 G A upstream_gene_variant MODIFIER c.-302C>T| S112
141018 BAA10g26120 A10 20825442 C T upstream_gene_variant MODIFIER c.-2541G>A| S107
141019 BAA10g26140 A10 20829870 G A downstream_gene_variant MODIFIER c.*1691C>T| S207
141020 BAA10g26140 A10 20830576 C T downstream_gene_variant MODIFIER c.*985G>A| S291
141021 BAA10g26140 A10 20831250 C T downstream_gene_variant MODIFIER c.*311G>A| S161
141022 BAA10g26140 A10 20831882 C T splice_acceptor_variant&intron_variant HIGH c.511-1G>A| S78
S83
141023 BAA10g26140 A10 20831940 G A intron_variant MODIFIER c.510+37C>T| S114
141024 BAA10g26140 A10 20832635 C T upstream_gene_variant MODIFIER c.-62G>A| S169
141025 BAA10g26140 A10 20833901 G A upstream_gene_variant MODIFIER c.-1328C>T| S55