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
114501 BAA10g09300 A10 11304087 C T upstream_gene_variant MODIFIER c.-3460G>A| S42
114502 BAA10g09300 A10 11304676 G A upstream_gene_variant MODIFIER c.-4049C>T| S112
114503 BAA10g09300 A10 11304945 C T upstream_gene_variant MODIFIER c.-4318G>A| S25
114504 BAA10g09310 A10 11305713 C T upstream_gene_variant MODIFIER c.-1540C>T| S149
114505 BAA10g09310 A10 11305716 C T upstream_gene_variant MODIFIER c.-1537C>T| S249
114506 BAA10g09310 A10 11306598 G A upstream_gene_variant MODIFIER c.-655G>A| S237
114507 BAA10g09310 A10 11306743 C T upstream_gene_variant MODIFIER c.-510C>T| S4
114508 BAA10g09310 A10 11307626 C T missense_variant MODERATE c.374C>T|p.Thr125Met S40
S49
114509 BAA10g09310 A10 11308063 C T stop_gained HIGH c.811C>T|p.Gln271* S173
114510 BAA10g09310 A10 11308697 G A missense_variant MODERATE c.1192G>A|p.Asp398Asn S68
114511 BAA10g09310 A10 11310325 C T synonymous_variant LOW c.2019C>T|p.Ile673Ile S287
114512 BAA10g09310 A10 11310419 C T missense_variant MODERATE c.2113C>T|p.His705Tyr S5
114513 BAA10g09310 A10 11310602 C T synonymous_variant LOW c.2296C>T|p.Leu766Leu S181
114514 BAA10g09310 A10 11310626 C T missense_variant MODERATE c.2320C>T|p.Leu774Phe S162
114515 BAA10g09310 A10 11310648 C T missense_variant MODERATE c.2342C>T|p.Ala781Val S196
114516 BAA10g09310 A10 11310954 G A downstream_gene_variant MODIFIER c.*182G>A| S150
114517 BAA10g09320 A10 11312778 C T synonymous_variant LOW c.552G>A|p.Gly184Gly S17
114518 BAA10g09320 A10 11313090 G A synonymous_variant LOW c.327C>T|p.Asp109Asp S18
114519 BAA10g09320 A10 11313308 C T missense_variant MODERATE c.109G>A|p.Glu37Lys S249
114520 BAA10g09320 A10 11313768 G A upstream_gene_variant MODIFIER c.-352C>T| S129
114521 BAA10g09320 A10 11314525 G A upstream_gene_variant MODIFIER c.-1109C>T| S72
S78
114522 BAA10g09320 A10 11314864 C T upstream_gene_variant MODIFIER c.-1448G>A| S51
114523 BAA10g09320 A10 11315199 G A upstream_gene_variant MODIFIER c.-1783C>T| S35
114524 BAA10g09320 A10 11315661 C T upstream_gene_variant MODIFIER c.-2245G>A| S128
114525 BAA10g09320 A10 11317856 C T upstream_gene_variant MODIFIER c.-4440G>A| S61