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
102001 BAA10g07370 A10 4233019 G A upstream_gene_variant MODIFIER c.-4602C>T| S273
S68
102002 BAA10g07370 A10 4233410 C T upstream_gene_variant MODIFIER c.-4993G>A| S271
102003 BAA10g07380 A10 4235086 G A upstream_gene_variant MODIFIER c.-2133C>T| S59
102004 BAA10g07380 A10 4235179 C T upstream_gene_variant MODIFIER c.-2226G>A| S202
102005 BAA10g07380 A10 4235816 C T upstream_gene_variant MODIFIER c.-2863G>A| S37
102006 BAA10g07380 A10 4235828 C T upstream_gene_variant MODIFIER c.-2875G>A| S177
102007 BAA10g07380 A10 4236421 C T upstream_gene_variant MODIFIER c.-3468G>A| S297
102008 BAA10g07380 A10 4236649 C T upstream_gene_variant MODIFIER c.-3696G>A| S155
S211
102009 BAA10g07380 A10 4236691 C T upstream_gene_variant MODIFIER c.-3738G>A| S266
102010 BAA10g07380 A10 4237348 C T upstream_gene_variant MODIFIER c.-4395G>A| S247
102011 BAA10g07380 A10 4237419 G A upstream_gene_variant MODIFIER c.-4466C>T| S75
S81
102012 BAA10g07380 A10 4237470 C T upstream_gene_variant MODIFIER c.-4517G>A| S159
S243
S299
102013 BAA10g07390 A10 4238757 G A downstream_gene_variant MODIFIER c.*975C>T| S9
102014 BAA10g07390 A10 4239016 C T downstream_gene_variant MODIFIER c.*716G>A| S265
102015 BAA10g07390 A10 4239293 G A downstream_gene_variant MODIFIER c.*439C>T| S198
102016 BAA10g07390 A10 4239726 G A downstream_gene_variant MODIFIER c.*6C>T| S205
102017 BAA10g07390 A10 4240922 C T splice_acceptor_variant&intron_variant HIGH c.274-1G>A| S281
102018 BAA10g07390 A10 4241205 C T missense_variant MODERATE c.67G>A|p.Ala23Thr S9
102019 BAA10g07390 A10 4241317 G A upstream_gene_variant MODIFIER c.-46C>T| S241
102020 BAA10g07390 A10 4241330 T C upstream_gene_variant MODIFIER c.-59A>G| S280
102021 BAA10g07400 A10 4242065 G A missense_variant MODERATE c.749C>T|p.Ala250Val S161
102022 BAA10g07400 A10 4242373 G A synonymous_variant LOW c.441C>T|p.Asn147Asn S228
102023 BAA10g07390 A10 4242566 C T upstream_gene_variant MODIFIER c.-1295G>A| S40
S49
102024 BAA10g07400 A10 4243056 C T synonymous_variant LOW c.123G>A|p.Gly41Gly S195
102025 BAA10g07390 A10 4243208 G A upstream_gene_variant MODIFIER c.-1937C>T| S228