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
101301 BAA10g07170 A10 4008241 C T upstream_gene_variant MODIFIER c.-3471G>A| S263
101302 BAA10g07170 A10 4008917 C T upstream_gene_variant MODIFIER c.-4147G>A| S25
101303 BAA10g07170 A10 4008962 C T upstream_gene_variant MODIFIER c.-4192G>A| S185
101304 BAA10g07180 A10 4010447 C T upstream_gene_variant MODIFIER c.-4570G>A| S84
S93
101305 BAA10g07200 A10 4012074 G A missense_variant MODERATE c.623G>A|p.Gly208Glu S69
101306 BAA10g07200 A10 4012116 G A missense_variant MODERATE c.665G>A|p.Gly222Glu S120
101307 BAA10g07200 A10 4012262 G A missense_variant MODERATE c.811G>A|p.Ala271Thr S164
101308 BAA10g07200 A10 4012827 G A missense_variant MODERATE c.1376G>A|p.Gly459Glu S125
101309 BAA10g07210 A10 4013398 C T downstream_gene_variant MODIFIER c.*2778G>A| S183
101310 BAA10g07210 A10 4014772 G A downstream_gene_variant MODIFIER c.*1404C>T| S303
101311 BAA10g07200 A10 4014923 G A downstream_gene_variant MODIFIER c.*47G>A| S53
101312 BAA10g07200 A10 4015118 C T downstream_gene_variant MODIFIER c.*242C>T| S260
101313 BAA10g07200 A10 4016069 G A downstream_gene_variant MODIFIER c.*1193G>A| S252
101314 BAA10g07200 A10 4016126 C T downstream_gene_variant MODIFIER c.*1250C>T| S40
S49
101315 BAA10g07200 A10 4016817 G A downstream_gene_variant MODIFIER c.*1941G>A| S120
101316 BAA10g07210 A10 4018266 G A upstream_gene_variant MODIFIER c.-1332C>T| S107
101317 BAA10g07210 A10 4018353 G A upstream_gene_variant MODIFIER c.-1419C>T| S295
101318 BAA10g07210 A10 4019994 G A upstream_gene_variant MODIFIER c.-3060C>T| S182
101319 BAA10g07210 A10 4020229 G A upstream_gene_variant MODIFIER c.-3295C>T| S230
101320 BAA10g07210 A10 4020355 G A upstream_gene_variant MODIFIER c.-3421C>T| S20
101321 BAA10g07210 A10 4020460 G A upstream_gene_variant MODIFIER c.-3526C>T| S164
101322 BAA10g07210 A10 4020645 C T upstream_gene_variant MODIFIER c.-3711G>A| S12
S266
101323 BAA10g07210 A10 4020654 G A upstream_gene_variant MODIFIER c.-3720C>T| S59
101324 BAA10g07210 A10 4021208 C T upstream_gene_variant MODIFIER c.-4274G>A| S297
101325 BAA10g07210 A10 4021644 C T upstream_gene_variant MODIFIER c.-4710G>A| S287