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
120401 BAA10g11830 A10 13404172 C T upstream_gene_variant MODIFIER c.-4408G>A| S164
120402 BAA10g11830 A10 13404327 G A upstream_gene_variant MODIFIER c.-4563C>T| S59
120403 BAA10g11840 A10 13405110 C T downstream_gene_variant MODIFIER c.*2862C>T| S84
S93
120404 BAA10g11840 A10 13405350 T A downstream_gene_variant MODIFIER c.*3102T>A| S172
120405 BAA10g11840 A10 13405508 C T downstream_gene_variant MODIFIER c.*3260C>T| S98
120406 BAA10g11840 A10 13406021 G A downstream_gene_variant MODIFIER c.*3773G>A| S136
120407 BAA10g11840 A10 13406678 C T downstream_gene_variant MODIFIER c.*4430C>T| S174
120408 BAA10g11840 A10 13406940 C T downstream_gene_variant MODIFIER c.*4692C>T| S152
120409 BAA10g11840 A10 13406941 C T downstream_gene_variant MODIFIER c.*4693C>T| S166
120410 BAA10g11840 A10 13407019 G T downstream_gene_variant MODIFIER c.*4771G>T| S171
120411 BAA10g11840 A10 13407174 G A downstream_gene_variant MODIFIER c.*4926G>A| S207
120412 BAA10g11850 A10 13411648 G A upstream_gene_variant MODIFIER c.-1125C>T| S202
120413 BAA10g11850 A10 13412611 C T upstream_gene_variant MODIFIER c.-2088G>A| S140
120414 BAA10g11850 A10 13412988 C T upstream_gene_variant MODIFIER c.-2465G>A| S177
120415 BAA10g11850 A10 13413236 C T upstream_gene_variant MODIFIER c.-2713G>A| S195
120416 BAA10g11860 A10 13413620 C T missense_variant MODERATE c.374C>T|p.Pro125Leu S114
120417 BAA10g11860 A10 13413666 G A synonymous_variant LOW c.420G>A|p.Gly140Gly S201
120418 BAA10g11860 A10 13413966 G A synonymous_variant LOW c.720G>A|p.Val240Val S130
120419 BAA10g11850 A10 13414919 G A upstream_gene_variant MODIFIER c.-4396C>T| S218
120420 BAA10g11850 A10 13415089 C T upstream_gene_variant MODIFIER c.-4566G>A| S276
120421 BAA10g11870 A10 13415751 C T downstream_gene_variant MODIFIER c.*1091G>A| S149
120422 BAA10g11870 A10 13416017 G A downstream_gene_variant MODIFIER c.*825C>T| S263
120423 BAA10g11860 A10 13416248 C T missense_variant MODERATE c.1727C>T|p.Pro576Leu S156
120424 BAA10g11860 A10 13416269 C T missense_variant MODERATE c.1748C>T|p.Ala583Val S122
120425 BAA10g11870 A10 13418367 G A missense_variant MODERATE c.689C>T|p.Ala230Val S271