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
131451 BAA10g18690 A10 17421243 C T synonymous_variant LOW c.1065G>A|p.Gly355Gly S194
131452 BAA10g18690 A10 17421297 G A synonymous_variant LOW c.1011C>T|p.Thr337Thr S293
131453 BAA10g18690 A10 17421726 C T synonymous_variant LOW c.582G>A|p.Arg194Arg S173
131454 BAA10g18690 A10 17421785 C T missense_variant MODERATE c.523G>A|p.Glu175Lys S177
131455 BAA10g18700 A10 17421915 C T upstream_gene_variant MODIFIER c.-1628C>T| S221
131456 BAA10g18690 A10 17421992 G A missense_variant MODERATE c.424C>T|p.Pro142Ser S16
131457 BAA10g18690 A10 17422002 C T synonymous_variant LOW c.414G>A|p.Arg138Arg S148
S30
S31
131458 BAA10g18700 A10 17422289 C T upstream_gene_variant MODIFIER c.-1254C>T| S45
131459 BAA10g18690 A10 17422339 C T synonymous_variant LOW c.195G>A|p.Arg65Arg S11
131460 BAA10g18690 A10 17422672 G A upstream_gene_variant MODIFIER c.-139C>T| S205
131461 BAA10g18690 A10 17425182 C T upstream_gene_variant MODIFIER c.-2649G>A| S51
131462 BAA10g18710 A10 17425658 C T missense_variant MODERATE c.466G>A|p.Val156Met S42
131463 BAA10g18710 A10 17426043 G A synonymous_variant LOW c.234C>T|p.Ser78Ser S169
131464 BAA10g18690 A10 17426855 C T upstream_gene_variant MODIFIER c.-4322G>A| S269
131465 BAA10g18690 A10 17427262 C T upstream_gene_variant MODIFIER c.-4729G>A| S203
131466 BAA10g18720 A10 17427517 G A stop_gained HIGH c.661C>T|p.Arg221* S111
131467 BAA10g18710 A10 17427642 C T upstream_gene_variant MODIFIER c.-1252G>A| S115
131468 BAA10g18720 A10 17428130 C T splice_acceptor_variant&intron_variant HIGH c.293-1G>A| S297
131469 BAA10g18720 A10 17428309 C T missense_variant MODERATE c.202G>A|p.Glu68Lys S238
131470 BAA10g18710 A10 17428590 C T upstream_gene_variant MODIFIER c.-2200G>A| S296
131471 BAA10g18710 A10 17430104 G A upstream_gene_variant MODIFIER c.-3714C>T| S16
131472 BAA10g18710 A10 17430385 C T upstream_gene_variant MODIFIER c.-3995G>A| S26
131473 BAA10g18730 A10 17430587 C T synonymous_variant LOW c.1380G>A|p.Arg460Arg S18
131474 BAA10g18730 A10 17430590 G A synonymous_variant LOW c.1377C>T|p.Tyr459Tyr S105
S106
131475 BAA10g18710 A10 17431098 C T upstream_gene_variant MODIFIER c.-4708G>A| S123