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
140451 BAA10g25620 A10 20623989 G A upstream_gene_variant MODIFIER c.-136C>T| S265
140452 BAA10g25620 A10 20624027 C T upstream_gene_variant MODIFIER c.-174G>A| S157
S163
140453 BAA10g25620 A10 20624376 G A upstream_gene_variant MODIFIER c.-523C>T| S175
140454 BAA10g25620 A10 20624925 T A upstream_gene_variant MODIFIER c.-1072A>T| S17
S218
S269
140455 BAA10g25620 A10 20625115 G A upstream_gene_variant MODIFIER c.-1262C>T| S280
140456 BAA10g25620 A10 20625419 G A upstream_gene_variant MODIFIER c.-1566C>T| S95
140457 BAA10g25640 A10 20626118 G A synonymous_variant LOW c.42G>A|p.Thr14Thr S63
140458 BAA10g25640 A10 20626228 G A missense_variant MODERATE c.152G>A|p.Arg51Gln S283
140459 BAA10g25640 A10 20626247 G A synonymous_variant LOW c.171G>A|p.Glu57Glu S90
140460 BAA10g25620 A10 20626476 C T upstream_gene_variant MODIFIER c.-2623G>A| S237
140461 BAA10g25640 A10 20626598 G A missense_variant MODERATE c.253G>A|p.Ala85Thr S74
140462 BAA10g25620 A10 20627013 C T upstream_gene_variant MODIFIER c.-3160G>A| S264
140463 BAA10g25620 A10 20627239 G A upstream_gene_variant MODIFIER c.-3386C>T| S127
140464 BAA10g25620 A10 20627288 C T upstream_gene_variant MODIFIER c.-3435G>A| S182
140465 BAA10g25620 A10 20628059 C T upstream_gene_variant MODIFIER c.-4206G>A| S144
140466 BAA10g25620 A10 20628546 G A upstream_gene_variant MODIFIER c.-4693C>T| S216
140467 BAA10g25650 A10 20629556 C T missense_variant MODERATE c.605C>T|p.Pro202Leu S157
140468 BAA10g25650 A10 20629814 C T missense_variant MODERATE c.743C>T|p.Ser248Leu S234
140469 BAA10g25630 A10 20630625 C T upstream_gene_variant MODIFIER c.-4595G>A| S20
140470 BAA10g25630 A10 20630714 C T upstream_gene_variant MODIFIER c.-4684G>A| S162
140471 BAA10g25630 A10 20630883 G A upstream_gene_variant MODIFIER c.-4853C>T| S62
140472 BAA10g25630 A10 20630989 G A upstream_gene_variant MODIFIER c.-4959C>T| S132
S137
S215
S89
140473 BAA10g25660 A10 20631147 C T upstream_gene_variant MODIFIER c.-301C>T| S276
140474 BAA10g25660 A10 20631306 C T upstream_gene_variant MODIFIER c.-142C>T| S230
140475 BAA10g25640 A10 20631787 C T downstream_gene_variant MODIFIER c.*4777C>T| S133
S202