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
131201 BAA10g18550 A10 17333579 C T downstream_gene_variant MODIFIER c.*1486G>A| S197
131202 BAA10g18550 A10 17333744 C T downstream_gene_variant MODIFIER c.*1321G>A| S156
131203 BAA10g18550 A10 17333858 C T downstream_gene_variant MODIFIER c.*1207G>A| S247
131204 BAA10g18550 A10 17334534 C T downstream_gene_variant MODIFIER c.*531G>A| S103
131205 BAA10g18550 A10 17334757 C T downstream_gene_variant MODIFIER c.*308G>A| S77
131206 BAA10g18550 A10 17335444 C T missense_variant MODERATE c.1724G>A|p.Arg575His S51
131207 BAA10g18550 A10 17335848 C T synonymous_variant LOW c.1320G>A|p.Lys440Lys S236
131208 BAA10g18550 A10 17336118 G A synonymous_variant LOW c.1050C>T|p.Ser350Ser S221
131209 BAA10g18550 A10 17336711 G A stop_gained HIGH c.457C>T|p.Gln153* S297
131210 BAA10g18550 A10 17336880 G A synonymous_variant LOW c.288C>T|p.Ser96Ser S151
S263
131211 BAA10g18550 A10 17337137 C T intron_variant MODIFIER c.211-180G>A| S183
131212 BAA10g18550 A10 17338040 C T intron_variant MODIFIER c.210+804G>A| S232
131213 BAA10g18550 A10 17338922 C T synonymous_variant LOW c.132G>A|p.Thr44Thr S283
131214 BAA10g18550 A10 17339136 G A upstream_gene_variant MODIFIER c.-83C>T| S293
131215 BAA10g18550 A10 17339191 G A upstream_gene_variant MODIFIER c.-138C>T| S63
131216 BAA10g18550 A10 17339765 C T upstream_gene_variant MODIFIER c.-712G>A| S195
131217 BAA10g18550 A10 17339994 G A upstream_gene_variant MODIFIER c.-941C>T| S198
131218 BAA10g18550 A10 17340256 C T upstream_gene_variant MODIFIER c.-1203G>A| S23
131219 BAA10g18550 A10 17341474 G A upstream_gene_variant MODIFIER c.-2421C>T| S293
131220 BAA10g18550 A10 17342323 G A upstream_gene_variant MODIFIER c.-3270C>T| S216
131221 BAA10g18560 A10 17344676 C T downstream_gene_variant MODIFIER c.*2206G>A| S237
131222 BAA10g18560 A10 17348034 G A intron_variant MODIFIER c.1455+53C>T| S7
131223 BAA10g18560 A10 17348510 C T missense_variant MODERATE c.1106G>A|p.Arg369Lys S23
S84
S93
131224 BAA10g18560 A10 17348523 C T missense_variant MODERATE c.1093G>A|p.Gly365Ser S297
131225 BAA10g18560 A10 17348620 C T stop_gained HIGH c.996G>A|p.Trp332* S188